A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635853



Internal ID7022650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23858758..23910239hg38UCSC Ensembl
Innerchr15:23859258..23909739hg38UCSC Ensembl
Outerchr15:23857758..23911239hg38UCSC Ensembl
chr15:24103905..24155386hg19UCSC Ensembl
Innerchr15:24104405..24154886hg19UCSC Ensembl
Outerchr15:24102905..24156386hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3851482
hg1951482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15182127
SamplesHG01672
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635853
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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