A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636335



Internal ID6676442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45245845..45247588hg38UCSC Ensembl
Innerchr15:45245895..45247538hg38UCSC Ensembl
Outerchr15:45245782..45247651hg38UCSC Ensembl
chr15:45538043..45539786hg19UCSC Ensembl
Innerchr15:45538093..45539736hg19UCSC Ensembl
Outerchr15:45537980..45539849hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381744
hg191744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15233829
SamplesHG03789
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636335
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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