A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15601062



Internal ID6500798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5868212..5887059hg38UCSC Ensembl
Innerchr17:5868712..5886559hg38UCSC Ensembl
Outerchr17:5867212..5888059hg38UCSC Ensembl
chr17:5771532..5790379hg19UCSC Ensembl
Innerchr17:5772032..5789879hg19UCSC Ensembl
Outerchr17:5770532..5791379hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3818848
hg1918848
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639823
Supporting Variants
SamplesNA20533
Known GenesLOC339166
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15601062
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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