A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6950211



Internal ID9707432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:43140507..43240078hg38UCSC Ensembl
Outerchr19:43644659..43744230hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3899572
hg1999572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718603, esv2718594, esv2718599, esv2718604
Supporting Variants
SamplesSSM024
Known GenesLOC284344, PSG4, PSG5
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)essv6950211
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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