A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515804



Internal ID15442861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172897975..172923635hg38UCSC Ensembl
Innerchr5:172324978..172350638hg19UCSC Ensembl
Innerchr5:172257584..172283244hg18UCSC Ensembl
Innerchr5:172257584..172283244hg17UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3825661
hg1925661
hg1825661
hg1725661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704411, nssv691991, nssv664831, nssv656845, nssv687503, nssv689520, nssv686685
Samples
Known GenesERGIC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515804
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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