A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15231053



Internal ID4582116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42553154..42554676hg38UCSC Ensembl
Innerchr15:42553154..42554676hg38UCSC Ensembl
Outerchr15:42552889..42554979hg38UCSC Ensembl
chr15:42845352..42846874hg19UCSC Ensembl
Innerchr15:42845352..42846874hg19UCSC Ensembl
Outerchr15:42845087..42847177hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg381523
hg191523
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636275
Supporting Variants
SamplesHG04096
Known GenesHAUS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15231053
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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