A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583022



Internal ID18881303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:168940550..168968473hg38UCSC Ensembl
Innerchr2:169797060..169824983hg19UCSC Ensembl
Innerchr2:169505306..169533229hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3827924
hg1927924
hg1827924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003689
Supporting Variants
Samples
Known GenesABCB11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3583022
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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