A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639976



Internal ID7026754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12652893..12661907hg38UCSC Ensembl
Innerchr17:12652908..12661892hg38UCSC Ensembl
Outerchr17:12652878..12661922hg38UCSC Ensembl
chr17:12556210..12565224hg19UCSC Ensembl
Innerchr17:12556225..12565209hg19UCSC Ensembl
Outerchr17:12556195..12565239hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg389015
hg199015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15613025
SamplesHG01790
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639976
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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