A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173810



Internal ID15873915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:31699894..31749577hg38UCSC Ensembl
Innerchr1:32165495..32215178hg19UCSC Ensembl
Innerchr1:31938082..31987765hg18UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3849684
hg1949684
hg1849684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545953
Supporting Variants
SamplesHGDP00433
Known GenesBAI2, COL16A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173810
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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