A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15261139



Internal ID2105363
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636654
Supporting Variants
SamplesHG01917
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15261139
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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