A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998510



Internal ID19158046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88876695..89025964hg38UCSC Ensembl
Innerchr2:89176211..89325461hg19UCSC Ensembl
Innerchr2:88957326..89106576hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38149270
hg19149251
hg18149251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3934n100
Supporting Variantsnssv3729928
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)nsv998510
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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