A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528881



Internal ID15456174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:9566439..9591164hg38UCSC Ensembl
Innerchr6:9566672..9591397hg19UCSC Ensembl
Innerchr6:9674658..9699383hg18UCSC Ensembl
Innerchr6:9674658..9699383hg17UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3824726
hg1924726
hg1824726
hg1724726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705561
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528881
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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