A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15292634



Internal ID1649153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73789134..73813236hg38UCSC Ensembl
chr15:74081475..74105577hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3824103
hg1924103
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636894
Supporting Variants
SamplesHG01516
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15292634
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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