A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6710391



Internal ID10121828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:56600155..56600554hg38UCSC Ensembl
Outerchr19:57111523..57111922hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2719039
Supporting Variants
SamplesSSM041
Known GenesZNF71
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)essv6710391
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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