A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636654



Internal ID7023448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60100171..60119064hg38UCSC Ensembl
Innerchr15:60100171..60119064hg38UCSC Ensembl
Outerchr15:60099671..60119564hg38UCSC Ensembl
chr15:60392370..60411263hg19UCSC Ensembl
Innerchr15:60392370..60411263hg19UCSC Ensembl
Outerchr15:60391870..60411763hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3818894
hg1918894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15261139
SamplesHG01917
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636654
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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