A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013068



Internal ID19102286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:163120676..163146011hg38UCSC Ensembl
Innerchr2:163977186..164002521hg19UCSC Ensembl
Innerchr2:163685432..163710767hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3825336
hg1925336
hg1825336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582996
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)nsv1013068
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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