A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6678895



Internal ID9745819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:52683377..52978659hg38UCSC Ensembl
Outerchr19:53186630..53481912hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38295283
hg19295283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2718787, esv2718796, esv2718786
Supporting Variants
SamplesSSM032
Known GenesZNF28, ZNF320, ZNF321P, ZNF468, ZNF600, ZNF611, ZNF702P, ZNF816, ZNF816-ZNF321P, 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)essv6678895
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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