A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637264



Internal ID7024058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92497399..92580554hg38UCSC Ensembl
chr15:93040629..93123784hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3883156
hg1983156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv460e214
Supporting Variantsessv15320968, essv15320967
SamplesNA20911, HG01597
Known GenesC15orf32, LINC00930
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637264
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer