A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559028



Internal ID15999751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:57201154..57209494hg38UCSC Ensembl
Innerchr12:57594937..57603277hg19UCSC Ensembl
Innerchr12:55881204..55889544hg18UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg388341
hg198341
hg188341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv796318
Samples
Known GenesLRP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559028
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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