A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6788879



Internal ID9846221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54725944..54818327hg38UCSC Ensembl
Outerchr19:55237410..55329782hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3892384
hg1992373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718911, esv2718872
Supporting Variants
SamplesSSM069
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)essv6788879
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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