A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15285125



Internal ID810987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71182063..71185594hg38UCSC Ensembl
Innerchr15:71182065..71185593hg38UCSC Ensembl
Outerchr15:71182062..71185596hg38UCSC Ensembl
chr15:71474402..71477933hg19UCSC Ensembl
Innerchr15:71474404..71477932hg19UCSC Ensembl
Outerchr15:71474401..71477935hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383532
hg193532
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636851
Supporting Variants
SamplesHG00384
Known GenesTHSD4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15285125
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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