A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15236967



Internal ID3974661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45843234..45971616hg38UCSC Ensembl
chr15:46135432..46263814hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38128383
hg19128383
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636350
Supporting Variants
SamplesHG03629
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15236967
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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