A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726740



Internal ID19025021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:5155756..5498040hg38UCSC Ensembl
Innerchr2:5295889..5638172hg19UCSC Ensembl
Innerchr2:5213340..5555623hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38342285
hg19342284
hg18342284
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000711
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)nssv3726740
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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