A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640921



Internal ID6681006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60062638..60064149hg38UCSC Ensembl
Innerchr17:60062652..60064135hg38UCSC Ensembl
Outerchr17:60062624..60064163hg38UCSC Ensembl
chr17:58139999..58141510hg19UCSC Ensembl
Innerchr17:58140013..58141496hg19UCSC Ensembl
Outerchr17:58139985..58141524hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg381512
hg191512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15714816
SamplesHG00113
Known GenesHEATR6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640921
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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