A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683449



Internal ID15420101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54227805..54239341hg38UCSC Ensembl
Innerchr19:54731679..54743217hg19UCSC Ensembl
Innerchr19:59423491..59435029hg18UCSC Ensembl
Innerchr19:59423491..59435029hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3811537
hg1911539
hg1811539
hg1711539
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517129
Supporting Variants
Samples
Known GenesLILRA6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683449
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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