A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637085



Internal ID7023879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84030462..84039199hg38UCSC Ensembl
Innerchr15:84030462..84039199hg38UCSC Ensembl
Outerchr15:84030275..84039468hg38UCSC Ensembl
chr15:84699214..84707951hg19UCSC Ensembl
Innerchr15:84699214..84707951hg19UCSC Ensembl
Outerchr15:84699027..84708220hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg388738
hg198738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15313596, essv15313597
SamplesHG00566, HG01807
Known GenesADAMTSL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637085
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