A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6782299



Internal ID9656070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54736409..54830541hg38UCSC Ensembl
Outerchr19:55247876..55341996hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3894133
hg1994121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718872, esv2718911, esv2718913
Supporting Variants
SamplesSSM008
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)essv6782299
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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