A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580170



Internal ID16367579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54225208..54239341hg38UCSC Ensembl
Innerchr19:54729079..54743217hg19UCSC Ensembl
Innerchr19:59420891..59435029hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3814134
hg1914139
hg1814139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6551n54
Supporting Variantsnssv901439, nssv901438, nssv901437
Samples
Known GenesLILRA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580170
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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