A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038960



Internal ID18781491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67960356..68018085hg38UCSC Ensembl
Innerchr11:67727827..67785555hg19UCSC Ensembl
Innerchr11:67484403..67542131hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3857730
hg1957729
hg1857729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710638
Samples
Known GenesALDH3B1, UNC93B1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038960
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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