A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636185



Internal ID7022981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38007936..38032983hg38UCSC Ensembl
Innerchr15:38007997..38032922hg38UCSC Ensembl
Outerchr15:38007875..38033044hg38UCSC Ensembl
chr15:38300137..38325184hg19UCSC Ensembl
Innerchr15:38300198..38325123hg19UCSC Ensembl
Outerchr15:38300076..38325245hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3825048
hg1925048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15220385, essv15220384, essv15220381, essv15220379, essv15220383, essv15220382, essv15220380
SamplesNA20905, HG03897, HG03585, HG01414, HG03858, HG03882, NA20827
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636185
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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