A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528939



Internal ID15456232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22273674..22281064hg38UCSC Ensembl
Innerchr1:22600167..22607557hg19UCSC Ensembl
Innerchr1:22472754..22480144hg18UCSC Ensembl
Innerchr1:22345473..22352863hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg387391
hg197391
hg187391
hg177391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705630
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528939
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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