A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580174



Internal ID16367583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54225208..54242931hg38UCSC Ensembl
Innerchr19:54729079..54746780hg19UCSC Ensembl
Innerchr19:59420891..59438592hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3817724
hg1917702
hg1817702
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6555n54
Supporting Variantsnssv901446, nssv901445
Samples
Known GenesLILRA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580174
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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