A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640182



Internal ID7026957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19756103..19759435hg38UCSC Ensembl
Innerchr17:19756138..19759401hg38UCSC Ensembl
Outerchr17:19756069..19759470hg38UCSC Ensembl
chr17:19659416..19662748hg19UCSC Ensembl
Innerchr17:19659451..19662714hg19UCSC Ensembl
Outerchr17:19659382..19662783hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg383333
hg193333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15648053
SamplesHG01806
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640182
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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