A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528681



Internal ID15455974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:12339802..12361987hg38UCSC Ensembl
Innerchr6:12340034..12362219hg19UCSC Ensembl
Innerchr6:12448020..12470205hg18UCSC Ensembl
Innerchr6:12448020..12470205hg17UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3822186
hg1922186
hg1822186
hg1722186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705323
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528681
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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