A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15345224



Internal ID3266271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99723812..99724352hg38UCSC Ensembl
Innerchr15:99723812..99724352hg38UCSC Ensembl
Outerchr15:99723444..99724653hg38UCSC Ensembl
chr15:100264017..100264557hg19UCSC Ensembl
Innerchr15:100264017..100264557hg19UCSC Ensembl
Outerchr15:100263649..100264858hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637431
Supporting Variants
SamplesHG02884
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15345224
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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