A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637096



Internal ID7023890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84629396..84636592hg38UCSC Ensembl
chr15:85172627..85179823hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg387197
hg197197
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15313628, essv15313629
SamplesHG02325, HG02885
Known GenesSCAND2P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637096
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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