A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15653086



Internal ID3446787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27241204..27242319hg38UCSC Ensembl
Innerchr17:27241400..27242269hg38UCSC Ensembl
Outerchr17:27241062..27242461hg38UCSC Ensembl
chr17:25568230..25569345hg19UCSC Ensembl
Innerchr17:25568426..25569295hg19UCSC Ensembl
Outerchr17:25568088..25569487hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg381116
hg191116
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640289
Supporting Variants
SamplesHG03077
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15653086
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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