A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053963



Internal ID19143182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15888971..15943171hg38UCSC Ensembl
Innerchr10:15930970..15985170hg19UCSC Ensembl
Innerchr10:15970976..16025176hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3854201
hg1954201
hg1854201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515270
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)nsv1053963
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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