A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528624



Internal ID15455917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:164892429..165274195hg38UCSC Ensembl
Innerchr5:164319435..164701201hg19UCSC Ensembl
Innerchr5:164252013..164633779hg18UCSC Ensembl
Innerchr5:164252013..164633779hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38381767
hg19381767
hg18381767
hg17381767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705254
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528624
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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