A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6189404



Internal ID9643474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8093536..8093918hg38UCSC Ensembl
Outerchr17:8093379..8094071hg38UCSC Ensembl
Innerchr17:7996854..7997236hg19UCSC Ensembl
Outerchr17:7996697..7997389hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38693
hg19693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659032
Supporting Variants
SamplesNA19376
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6189404
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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