A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6868479



Internal ID9918427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54828126..54862158hg38UCSC Ensembl
Outerchr19:55339581..55373613hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3834033
hg1934033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718931, esv2718872
Supporting Variants
SamplesSSM089
Known GenesKIR2DS4, KIR3DL1, KIR3DL2
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6868479
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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