A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv796313



Internal ID16090269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:57200816..57205106hg38UCSC Ensembl
Innerchr12:57594599..57598889hg19UCSC Ensembl
Innerchr12:55880866..55885156hg18UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg384291
hg194291
hg184291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559025
Supporting Variants
Samples
Known GenesLRP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv796313
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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