A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6921441



Internal ID9684887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54736415..54830593hg38UCSC Ensembl
Outerchr19:55247882..55342048hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3894179
hg1994167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718913, esv2718911, esv2718872
Supporting Variants
SamplesSSM017
Known GenesKIR2DL1, KIR2DL3, KIR2DL4, KIR3DL1, KIR3DL3, LOC100287534
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)essv6921441
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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