A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001896



Internal ID19091113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14192011..14232559hg38UCSC Ensembl
Innerchr2:14332136..14372683hg19UCSC Ensembl
Innerchr2:14249587..14290134hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3840549
hg1940548
hg1840548
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3723n100
Supporting Variantsnssv3577058
Samples
Known GenesLINC00276
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001896
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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