A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640476



Internal ID7027251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36635237..36642007hg38UCSC Ensembl
Innerchr17:36635259..36641986hg38UCSC Ensembl
Outerchr17:36635216..36642029hg38UCSC Ensembl
chr17:34991695..34998463hg19UCSC Ensembl
Innerchr17:34991717..34998442hg19UCSC Ensembl
Outerchr17:34991674..34998485hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386771
hg196769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15666460
SamplesHG04022
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640476
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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