A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699538



Internal ID15436190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54637036..54666689hg38UCSC Ensembl
Innerchr19:55148487..55178140hg19UCSC Ensembl
Innerchr19:59840299..59869952hg18UCSC Ensembl
Innerchr19:59840299..59869952hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3829654
hg1929654
hg1829654
hg1729654
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523723
Supporting Variants
Samples
Known GenesLILRB1, LILRB4, MIR8061
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699538
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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