A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631664



Internal ID7018472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30042916..30045653hg38UCSC Ensembl
Innerchr13:30042942..30045627hg38UCSC Ensembl
Outerchr13:30042890..30045679hg38UCSC Ensembl
chr13:30617053..30619790hg19UCSC Ensembl
Innerchr13:30617079..30619764hg19UCSC Ensembl
Outerchr13:30617027..30619816hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg382738
hg192738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14680753
SamplesHG03777
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631664
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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