A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6828440



Internal ID10229079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:82976722..82976927hg38UCSC Ensembl
Outerchr17:80934598..80934803hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2716576, esv2716575
Supporting Variants
SamplesSSM080
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)essv6828440
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