A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14869665



Internal ID2065681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97603395..97610730hg38UCSC Ensembl
Innerchr13:97603445..97610680hg38UCSC Ensembl
Outerchr13:97603318..97610807hg38UCSC Ensembl
chr13:98255649..98262984hg19UCSC Ensembl
Innerchr13:98255699..98262934hg19UCSC Ensembl
Outerchr13:98255572..98263061hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg387336
hg197336
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633296
Supporting Variants
SamplesHG01882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14869665
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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