A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640654



Internal ID6680741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44732991..44741121hg38UCSC Ensembl
Innerchr17:44733141..44740971hg38UCSC Ensembl
Outerchr17:44732841..44741271hg38UCSC Ensembl
chr17:42810359..42818489hg19UCSC Ensembl
Innerchr17:42810509..42818339hg19UCSC Ensembl
Outerchr17:42810209..42818639hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg388131
hg198131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15680780
SamplesHG00707
Known GenesDBF4B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640654
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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