A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173785



Internal ID15532423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16203554..16334932hg38UCSC Ensembl
Innerchr1:16530049..16661427hg19UCSC Ensembl
Innerchr1:16402636..16534014hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38131379
hg19131379
hg18131379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545641
Supporting Variants
SamplesHGDP01309
Known GenesARHGEF19, FBXO42, RSG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173785
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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