A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3491250



Internal ID19078891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8658738..8687776hg38UCSC Ensembl
Innerchr10:8700701..8729739hg19UCSC Ensembl
Innerchr10:8740707..8769745hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3829039
hg1929039
hg1829039
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046158
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)nssv3491250
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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