A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052867



Internal ID19142086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:36907878..37034874hg38UCSC Ensembl
Innerchr10:37196806..37323802hg19UCSC Ensembl
Innerchr10:37236812..37363808hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38126997
hg19126997
hg18126997
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520678
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)nsv1052867
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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