A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6941115



Internal ID10049033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:71928589..71928758hg38UCSC Ensembl
Outerchr17:69924730..69924899hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2716175, esv2716176
Supporting Variants
SamplesSSM022
Known Genes
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)essv6941115
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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