A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515617



Internal ID15443228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:41322720..41325311hg38UCSC Ensembl
Innerchr6:41290458..41293049hg19UCSC Ensembl
Innerchr6:41398436..41401027hg18UCSC Ensembl
Innerchr6:41398436..41401027hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg382592
hg192592
hg182592
hg172592
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv670766, nssv691273, nssv657462, nssv662090, nssv664115, nssv706007, nssv665398
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515617
Frequency
Sample Size2026
Observed Gain3
Observed Loss4
Observed Complex0
Frequencyn/a


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