A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045736



Internal ID19134955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65798369..65847534hg38UCSC Ensembl
Innerchr10:67558127..67607292hg19UCSC Ensembl
Innerchr10:67228133..67277298hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3849166
hg1949166
hg1849166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515508
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)nsv1045736
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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