A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580172



Internal ID16367581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54225208..54240481hg38UCSC Ensembl
Innerchr19:54729079..54744358hg19UCSC Ensembl
Innerchr19:59420891..59436170hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3815274
hg1915280
hg1815280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6551n54
Supporting Variantsnssv901442, nssv901443
Samples
Known GenesLILRA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580172
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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