A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640806



Internal ID7027580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53781624..53792758hg38UCSC Ensembl
Innerchr17:53781674..53792708hg38UCSC Ensembl
Outerchr17:53781574..53792808hg38UCSC Ensembl
chr17:51858985..51870119hg19UCSC Ensembl
Innerchr17:51859035..51870069hg19UCSC Ensembl
Outerchr17:51858935..51870169hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3811135
hg1911135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15700311, essv15700310
SamplesHG03902, HG02604
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640806
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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