A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695654



Internal ID15432306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9753325..9768985hg38UCSC Ensembl
Innerchr2:9893454..9909114hg19UCSC Ensembl
Innerchr2:9810905..9826565hg18UCSC Ensembl
Innerchr2:9844052..9859712hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3815661
hg1915661
hg1815661
hg1715661
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518227
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695654
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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