A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15331120



Internal ID1277193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97059057..97081454hg38UCSC Ensembl
Innerchr15:97059057..97081454hg38UCSC Ensembl
Outerchr15:97058557..97081954hg38UCSC Ensembl
chr15:97602287..97624684hg19UCSC Ensembl
Innerchr15:97602287..97624684hg19UCSC Ensembl
Outerchr15:97601787..97625184hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3822398
hg1922398
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637363
Supporting Variants
SamplesHG01124
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15331120
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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