A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708742



Internal ID16002698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2267618..2300024hg38UCSC Ensembl
Innerchr1:2199057..2231463hg19UCSC Ensembl
Innerchr1:2188917..2221323hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3832407
hg1932407
hg1832407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545070
Supporting Variants
Samples
Known GenesSKI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708742
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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