A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6885629



Internal ID9933686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:76895665..76896142hg38UCSC Ensembl
Outerchr18:74607621..74608098hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2717421, esv2717388
Supporting Variants
SamplesSSM095
Known GenesZNF236
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)essv6885629
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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