A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2715379



Internal ID10299015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:893537..893692hg38UCSC Ensembl
Outerchr17:796777..796932hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6858170, essv6966825, essv6960348, essv6820400
SamplesSSM027, SSM087, SSM026, SSM078
Known GenesNXN
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)esv2715379
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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