A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636629



Internal ID6676736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58429372..58438600hg38UCSC Ensembl
Innerchr15:58429522..58438450hg38UCSC Ensembl
Outerchr15:58429222..58438750hg38UCSC Ensembl
chr15:58721571..58730799hg19UCSC Ensembl
Innerchr15:58721721..58730649hg19UCSC Ensembl
Outerchr15:58721421..58730949hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg389229
hg199229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15260071
SamplesHG02982
Known GenesLIPC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636629
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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