A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039988



Internal ID19129207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65534804..65568671hg38UCSC Ensembl
Innerchr10:67294562..67328429hg19UCSC Ensembl
Innerchr10:66964568..66998435hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3833868
hg1933868
hg1833868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv883n100
Supporting Variantsnssv3511631
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)nsv1039988
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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