A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692200



Internal ID15428852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9475244..9479634hg38UCSC Ensembl
Innerchr1:9535303..9539693hg19UCSC Ensembl
Innerchr1:9457890..9462280hg18UCSC Ensembl
Innerchr1:9469569..9473959hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg384391
hg194391
hg184391
hg174391
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517755
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692200
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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