A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14869725



Internal ID5878751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97757651..97758154hg38UCSC Ensembl
Innerchr13:97757651..97758154hg38UCSC Ensembl
Outerchr13:97757375..97758459hg38UCSC Ensembl
chr13:98409905..98410408hg19UCSC Ensembl
Innerchr13:98409905..98410408hg19UCSC Ensembl
Outerchr13:98409629..98410713hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633299
Supporting Variants
SamplesNA19307
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14869725
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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