A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15213179



Internal ID5214995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35225355..35227584hg38UCSC Ensembl
Innerchr15:35225371..35227568hg38UCSC Ensembl
Outerchr15:35225339..35227600hg38UCSC Ensembl
chr15:35517556..35519785hg19UCSC Ensembl
Innerchr15:35517572..35519769hg19UCSC Ensembl
Outerchr15:35517540..35519801hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382230
hg192230
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636131
Supporting Variants
SamplesHG03995
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15213179
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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