A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1028961



Internal ID15535461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:37206519..37409477hg38UCSC Ensembl
Innerchr5:37206621..37409579hg19UCSC Ensembl
Innerchr5:37242378..37445336hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38202959
hg19202959
hg18202959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597824
Supporting Variants
Samples
Known GenesC5orf42, NUP155, WDR70
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1028961
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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