A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636972



Internal ID7023766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77585594..77586798hg38UCSC Ensembl
Innerchr15:77585609..77586783hg38UCSC Ensembl
Outerchr15:77585579..77586813hg38UCSC Ensembl
chr15:77877936..77879140hg19UCSC Ensembl
Innerchr15:77877951..77879125hg19UCSC Ensembl
Outerchr15:77877921..77879155hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg381205
hg191205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15300734
SamplesHG00446
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636972
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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