A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640326



Internal ID7027101
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15657015, essv15657014, essv15657018, essv15657016, essv15657017
SamplesHG01710, NA12889, HG01700, NA20902, HG01786
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640326
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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