A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15664571



Internal ID5666387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35867758..35872823hg38UCSC Ensembl
Innerchr17:35867758..35872823hg38UCSC Ensembl
Outerchr17:35867258..35873323hg38UCSC Ensembl
chr17:34194762..34199827hg19UCSC Ensembl
Innerchr17:34194762..34199827hg19UCSC Ensembl
Outerchr17:34194262..34200327hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg385066
hg195066
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640458
Supporting Variants
SamplesHG01695
Known GenesC17orf66, CCL5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15664571
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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