A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6773182



Internal ID9831374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:52570227..53333668hg38UCSC Ensembl
Outerchr19:53073480..53836921hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38763442
hg19763442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718787
Supporting Variants
SamplesSSM065
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
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)essv6773182
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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