A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2716013



Internal ID9950300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:48223905..48224047hg38UCSC Ensembl
Outerchr17:46301267..46301409hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6905565
SamplesSSM013
Known GenesSKAP1
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)esv2716013
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer