A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641193



Internal ID7027967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72302922..72303867hg38UCSC Ensembl
Innerchr17:72302972..72303817hg38UCSC Ensembl
Outerchr17:72302872..72303917hg38UCSC Ensembl
chr17:70299063..70300008hg19UCSC Ensembl
Innerchr17:70299113..70299958hg19UCSC Ensembl
Outerchr17:70299013..70300058hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv586e214
Supporting Variantsessv15734913
SamplesNA20869
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641193
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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