A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15650660



Internal ID3018928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21047734..21057114hg38UCSC Ensembl
Innerchr17:21047734..21057114hg38UCSC Ensembl
Outerchr17:21047461..21057304hg38UCSC Ensembl
chr17:20951047..20960427hg19UCSC Ensembl
Innerchr17:20951047..20960427hg19UCSC Ensembl
Outerchr17:20950774..20960617hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg389381
hg199381
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640225
Supporting Variants
SamplesHG02657
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15650660
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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