A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv743474



Internal ID15690744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5163474..5590097hg38UCSC Ensembl
Innerchr10:5205437..5632060hg19UCSC Ensembl
Innerchr10:5195437..5622060hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38426624
hg19426624
hg18426624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549886
Supporting Variants
Samples
Known GenesAKR1C4, AKR1CL1, CALML3, CALML5, NET1, TUBAL3, UCN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv743474
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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