A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669739



Internal ID15406391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22173037..22180358hg38UCSC Ensembl
Innerchr1:22499530..22506851hg19UCSC Ensembl
Innerchr1:22372117..22379438hg18UCSC Ensembl
Innerchr1:22244836..22252157hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg387322
hg197322
hg187322
hg177322
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517086
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669739
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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