A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707767



Internal ID19006048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42118976..42272183hg38UCSC Ensembl
Innerchr10:42614424..42767631hg19UCSC Ensembl
Innerchr10:41934430..42087637hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38153208
hg19153208
hg18153208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038298
Supporting Variants
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)nssv3707767
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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