A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6842142



Internal ID9661211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:52570219..53333819hg38UCSC Ensembl
Outerchr19:53073472..53837072hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38763601
hg19763601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718787
Supporting Variants
SamplesSSM010
Known GenesBIRC8, ERVV-1, ERVV-2, FAM90A27P, VN1R2, VN1R4, ZNF137P, ZNF160, ZNF28, ZNF320, ZNF321P, ZNF347, ZNF415, ZNF468, ZNF600, ZNF611, ZNF665, ZNF677, ZNF701, ZNF702P, ZNF816, ZNF816-ZNF321P, ZNF818P, ZNF83, ZNF845
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)essv6842142
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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