A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636862



Internal ID6676969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71688229..71699359hg38UCSC Ensembl
Innerchr15:71688379..71699209hg38UCSC Ensembl
Outerchr15:71688079..71699509hg38UCSC Ensembl
chr15:71980568..71991698hg19UCSC Ensembl
Innerchr15:71980718..71991548hg19UCSC Ensembl
Outerchr15:71980418..71991848hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3811131
hg1911131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15287959, essv15287960, essv15287961
SamplesHG00632, HG02082, HG00864
Known GenesTHSD4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636862
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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