A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003853



Internal ID19093071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:164955918..165014191hg38UCSC Ensembl
Innerchr2:165812428..165870701hg19UCSC Ensembl
Innerchr2:165520674..165578947hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3858274
hg1958274
hg1858274
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3583003
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)nsv1003853
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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