A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15354195



Internal ID2049371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101213297..101216209hg38UCSC Ensembl
Innerchr15:101213447..101216059hg38UCSC Ensembl
Outerchr15:101213147..101216359hg38UCSC Ensembl
chr15:101753502..101756414hg19UCSC Ensembl
Innerchr15:101753652..101756264hg19UCSC Ensembl
Outerchr15:101753352..101756564hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382913
hg192913
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637503
Supporting Variants
SamplesHG01872
Known GenesCHSY1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15354195
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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