A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173797



Internal ID15881158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21923096..21958002hg38UCSC Ensembl
Innerchr1:22249589..22284495hg19UCSC Ensembl
Innerchr1:22122176..22157082hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3834907
hg1934907
hg1834907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545744
Supporting Variants
SamplesNINDS_74
Known GenesHSPG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173797
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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