A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3723n100



Internal ID22789810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14192011..14232559hg38UCSC Ensembl
chr2:14332136..14372683hg19UCSC Ensembl
chr2:14249587..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 Variants
Supporting Variantsnsv1001896, nsv997320
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)dgv3723n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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