A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437751



Internal ID15036483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:42196422..42197093hg38UCSC Ensembl
Outerchr12:42192839..42205320hg38UCSC Ensembl
Innerchr12:42590224..42590895hg19UCSC Ensembl
Outerchr12:42586641..42599122hg19UCSC Ensembl
Innerchr12:40876491..40877162hg18UCSC Ensembl
Outerchr12:40872908..40885389hg18UCSC Ensembl
Innerchr12:40876491..40877162hg16UCSC Ensembl
Outerchr12:40872908..40885389hg16UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3812482
hg1912482
hg1812482
hg1612482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467632
SamplesNA19094
Known GenesYAF2
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nsv437751
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer