A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174139



Internal ID15873844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18550421..18617006hg38UCSC Ensembl
Innerchr10:18839350..18905935hg19UCSC Ensembl
Innerchr10:18879356..18945941hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3866586
hg1966586
hg1866586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550044
Supporting Variants
SamplesHGDP00397
Known GenesNSUN6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174139
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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