A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525621



Internal ID15452914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:9590543..9765660hg38UCSC Ensembl
Innerchr6:9590776..9765893hg19UCSC Ensembl
Innerchr6:9698762..9873879hg18UCSC Ensembl
Innerchr6:9698762..9873879hg17UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38175118
hg19175118
hg18175118
hg17175118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701767
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525621
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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