A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6835900



Internal ID9888919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:52519391..52847499hg38UCSC Ensembl
Outerchr19:53022644..53350752hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38328109
hg19328109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718786
Supporting Variants
SamplesSSM082
Known GenesZNF137P, ZNF28, ZNF468, ZNF600, ZNF611, ZNF701, ZNF808, ZNF83
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)essv6835900
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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