A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559031



Internal ID15999754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:57203386..57208298hg38UCSC Ensembl
Innerchr12:57597169..57602081hg19UCSC Ensembl
Innerchr12:55883436..55888348hg18UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg384913
hg194913
hg184913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv796321
Samples
Known GenesLRP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559031
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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