A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15657015



Internal ID1847691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29388153..29388953hg38UCSC Ensembl
Innerchr17:29388277..29388903hg38UCSC Ensembl
Outerchr17:29388103..29389003hg38UCSC Ensembl
chr17:27715171..27715971hg19UCSC Ensembl
Innerchr17:27715295..27715921hg19UCSC Ensembl
Outerchr17:27715121..27716021hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640326
Supporting Variants
SamplesHG01710
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15657015
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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