A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726656



Internal ID19024937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:847575..1104354hg38UCSC Ensembl
Innerchr2:843607..1100040hg19UCSC Ensembl
Innerchr2:833607..1090040hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38256780
hg19256434
hg18256434
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998964
Supporting Variants
Samples
Known GenesLINC01115, SNTG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726656
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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