A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv719702



Internal ID16013658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102711036..102802203hg38UCSC Ensembl
Innerchr1:103176592..103267759hg19UCSC Ensembl
Innerchr1:102949180..103040347hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3891168
hg1991168
hg1891168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546925
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv719702
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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