A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729275



Internal ID19027556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:176355304..176426029hg38UCSC Ensembl
Innerchr2:177220032..177290757hg19UCSC Ensembl
Innerchr2:176928278..176999003hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3870726
hg1970726
hg1870726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015076
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3729275
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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