A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998161



Internal ID19157698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:78177223..78433039hg38UCSC Ensembl
Innerchr2:78404349..78660165hg19UCSC Ensembl
Innerchr2:78257857..78513673hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38255817
hg19255817
hg18255817
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3880n100
Supporting Variantsnssv3582107
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)nsv998161
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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