A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632685



Internal ID7019496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71964012..71967928hg38UCSC Ensembl
Innerchr13:71964062..71967878hg38UCSC Ensembl
Outerchr13:71963962..71967978hg38UCSC Ensembl
chr13:72538150..72542066hg19UCSC Ensembl
Innerchr13:72538200..72542016hg19UCSC Ensembl
Outerchr13:72538100..72542116hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg383917
hg193917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14791346
SamplesHG02425
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632685
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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