A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636695



Internal ID6676802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62255972..62260221hg38UCSC Ensembl
Innerchr15:62256022..62260171hg38UCSC Ensembl
Outerchr15:62255858..62260335hg38UCSC Ensembl
chr15:62548171..62552420hg19UCSC Ensembl
Innerchr15:62548221..62552370hg19UCSC Ensembl
Outerchr15:62548057..62552534hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg384250
hg194250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15266015, essv15266022, essv15266024, essv15266020, essv15266018, essv15266025, essv15266016, essv15266027, essv15266017, essv15266021, essv15266023, essv15266026, essv15266019
SamplesHG00242, HG02688, NA21128, HG03757, NA20911, HG03887, HG03910, NA21114, HG03829, NA20867, NA21143, NA21087, HG03729
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636695
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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