A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528949



Internal ID15456242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:41675648..41676703hg38UCSC Ensembl
Innerchr6:41643386..41644441hg19UCSC Ensembl
Innerchr6:41751364..41752419hg18UCSC Ensembl
Innerchr6:41751364..41752419hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381056
hg191056
hg181056
hg171056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705643
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528949
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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