A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013061



Internal ID19102279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:17979658..18018882hg38UCSC Ensembl
Innerchr2:18160924..18200148hg19UCSC Ensembl
Innerchr2:18024405..18063629hg18UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3839225
hg1939225
hg1839225
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3578931
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)nsv1013061
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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