A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641213



Internal ID7027987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73179289..73182151hg38UCSC Ensembl
Innerchr17:73179302..73182139hg38UCSC Ensembl
Outerchr17:73179277..73182164hg38UCSC Ensembl
chr17:71175428..71178290hg19UCSC Ensembl
Innerchr17:71175441..71178278hg19UCSC Ensembl
Outerchr17:71175416..71178303hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg382863
hg192863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15735965, essv15735964
SamplesNA19031, NA20758
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641213
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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