A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013617



Internal ID18756149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:98326914..98387710hg38UCSC Ensembl
Innerchr2:98943377..99004173hg19UCSC Ensembl
Innerchr2:98309809..98370605hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3860797
hg1960797
hg1860797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3729165
Samples
Known GenesCNGA3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013617
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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