A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6921446



Internal ID9684892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54826951..54844889hg38UCSC Ensembl
Outerchr19:55338406..55356344hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3817939
hg1917939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718931, esv2718920, esv2718872, esv2718913
Supporting Variants
SamplesSSM017
Known GenesKIR2DS4, KIR3DL1
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)essv6921446
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer