A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041840



Internal ID19131059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65635564..65695093hg38UCSC Ensembl
Innerchr10:67395322..67454851hg19UCSC Ensembl
Innerchr10:67065328..67124857hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3859530
hg1959530
hg1859530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508712
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)nsv1041840
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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