A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661187



Internal ID15051153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:33533389..33540888hg38UCSC Ensembl
Innerchr2:33758456..33765955hg19UCSC Ensembl
Innerchr2:33611960..33619459hg18UCSC Ensembl
Innerchr2:33670107..33677606hg17UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg387500
hg197500
hg187500
hg177500
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516338
Supporting Variants
Samples
Known GenesRASGRP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661187
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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