A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15734818



Internal ID5736634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71833004..71837062hg38UCSC Ensembl
Innerchr17:71833004..71837062hg38UCSC Ensembl
Outerchr17:71832805..71837420hg38UCSC Ensembl
chr17:69829145..69833203hg19UCSC Ensembl
Innerchr17:69829145..69833203hg19UCSC Ensembl
Outerchr17:69828946..69833561hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg384059
hg194059
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641180
Supporting Variants
SamplesHG03756
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15734818
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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