A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515501



Internal ID15443112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26444384..26455546hg38UCSC Ensembl
Innerchr4:26446006..26457168hg19UCSC Ensembl
Innerchr4:26055104..26066266hg18UCSC Ensembl
Innerchr4:26122275..26133437hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3811163
hg1911163
hg1811163
hg1711163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686846, nssv653344, nssv693386, nssv695006, nssv658937, nssv680721, nssv655736, nssv700606, nssv657507
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515501
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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