A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698613



Internal ID15435265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54600262..54600320hg38UCSC Ensembl
Innerchr19:55111727..55111785hg19UCSC Ensembl
Innerchr19:59803539..59803597hg18UCSC Ensembl
Innerchr19:59803539..59803597hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3859
hg1959
hg1859
hg1759
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516569
Supporting Variants
Samples
Known GenesLILRA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698613
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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