A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv436933



Internal ID15383174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10125354..10126522hg38UCSC Ensembl
Outerchr4:10123631..10130308hg38UCSC Ensembl
Innerchr4:10126978..10128146hg19UCSC Ensembl
Outerchr4:10125255..10131932hg19UCSC Ensembl
Innerchr4:9736076..9737244hg18UCSC Ensembl
Outerchr4:9734353..9741030hg18UCSC Ensembl
Innerchr4:9877861..9879029hg16UCSC Ensembl
Outerchr4:9876138..9882815hg16UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg386678
hg196678
hg186678
hg166678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv466814
SamplesNA10830
Known Genes
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)nsv436933
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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