A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437786



Internal ID15383092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:50747649..50753804hg38UCSC Ensembl
Outerchr13:50744439..50757414hg38UCSC Ensembl
Innerchr13:51321785..51327940hg19UCSC Ensembl
Outerchr13:51318575..51331550hg19UCSC Ensembl
Innerchr13:50219786..50225941hg18UCSC Ensembl
Outerchr13:50216576..50229551hg18UCSC Ensembl
Innerchr13:49119786..49125941hg16UCSC Ensembl
Outerchr13:49116576..49129551hg16UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3812976
hg1912976
hg1812976
hg1612976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467667
SamplesNA19161
Known GenesDLEU7
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)nsv437786
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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