A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6832034



Internal ID10232311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:82976721..82976920hg38UCSC Ensembl
Outerchr17:80934597..80934796hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2716576, esv2716575
Supporting Variants
SamplesSSM081
Known GenesB3GNTL1
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)essv6832034
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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