A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6405204



Internal ID9566139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8093481..8093955hg38UCSC Ensembl
Outerchr17:8093430..8094008hg38UCSC Ensembl
Innerchr17:7996799..7997273hg19UCSC Ensembl
Outerchr17:7996748..7997326hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674527
Supporting Variants
SamplesNA19114
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6405204
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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