A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6721749



Internal ID9783268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54812701..54829013hg38UCSC Ensembl
Outerchr19:55324156..55340468hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3816313
hg1916313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718920, esv2718926, esv2718872, esv2718913, esv2718930
Supporting Variants
SamplesSSM044
Known GenesKIR2DL4, KIR3DL1, 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)essv6721749
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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