A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010496



Internal ID19099713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:207479254..207495060hg38UCSC Ensembl
Innerchr2:208343978..208359784hg19UCSC Ensembl
Innerchr2:208052223..208068029hg18UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3815807
hg1915807
hg1815807
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4158n100
Supporting Variantsnssv3585595
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)nsv1010496
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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