A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3576633



Internal ID18528228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:54065814..54116329hg38UCSC Ensembl
Innerchr2:54292951..54343466hg19UCSC Ensembl
Innerchr2:54146455..54196970hg18UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3850516
hg1950516
hg1850516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010175
Supporting Variants
Samples
Known GenesACYP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3576633
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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