A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999881



Internal ID17292833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54238725..54256437hg38UCSC Ensembl
Outerchr19:54742601..54760300hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3817713
hg1917700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953615
Supporting Variants
SamplesBILGI_BIOE
Known GenesLILRA6, LILRB5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999881
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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