A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15655822



Internal ID2067930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27948898..27949816hg38UCSC Ensembl
Innerchr17:27948912..27949803hg38UCSC Ensembl
Outerchr17:27948885..27949830hg38UCSC Ensembl
chr17:26275924..26276842hg19UCSC Ensembl
Innerchr17:26275938..26276829hg19UCSC Ensembl
Outerchr17:26275911..26276856hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640302
Supporting Variants
SamplesHG01882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15655822
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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