A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15188728



Internal ID5297002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25647036..25649837hg38UCSC Ensembl
Innerchr15:25647036..25649837hg38UCSC Ensembl
Outerchr15:25646927..25649843hg38UCSC Ensembl
chr15:25892183..25894984hg19UCSC Ensembl
Innerchr15:25892183..25894984hg19UCSC Ensembl
Outerchr15:25892074..25894990hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg382802
hg192802
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635932
Supporting Variants
SamplesNA18749
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15188728
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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