A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050867



Internal ID19140086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63507887..63545394hg38UCSC Ensembl
Innerchr13:64082020..64119527hg19UCSC Ensembl
Innerchr13:62980021..63017528hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3837508
hg1937508
hg1837508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3711771
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050867
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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