A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640614



Internal ID7027389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42887870..42897271hg38UCSC Ensembl
Innerchr17:42888020..42897121hg38UCSC Ensembl
Outerchr17:42887720..42897421hg38UCSC Ensembl
chr17:41039887..41049288hg19UCSC Ensembl
Innerchr17:41040037..41049138hg19UCSC Ensembl
Outerchr17:41039737..41049438hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg389402
hg199402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15679107
SamplesHG02613
Known GenesLINC00671
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640614
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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