A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15198891



Internal ID1004034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28108015..28121432hg38UCSC Ensembl
chr15:28353161..28366578hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3813418
hg1913418
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635989
Supporting Variants
SamplesHG00628
Known GenesHERC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15198891
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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