A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15267691



Internal ID2704188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62551608..62595341hg38UCSC Ensembl
Innerchr15:62551631..62595318hg38UCSC Ensembl
Outerchr15:62551585..62595364hg38UCSC Ensembl
chr15:62843807..62887540hg19UCSC Ensembl
Innerchr15:62843830..62887517hg19UCSC Ensembl
Outerchr15:62843784..62887563hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3843734
hg1943734
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636702
Supporting Variants
SamplesHG02389
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15267691
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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