A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv744252



Internal ID16038208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18561034..18571209hg38UCSC Ensembl
Innerchr10:18849963..18860138hg19UCSC Ensembl
Innerchr10:18889969..18900144hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3810176
hg1910176
hg1810176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550100
Supporting Variants
Samples
Known GenesNSUN6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv744252
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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