A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15313624



Internal ID3267691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84578829..84607494hg38UCSC Ensembl
chr15:85122060..85150725hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3828666
hg1928666
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637093
Supporting Variants
SamplesHG02885
Known GenesLINC00933, ZSCAN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15313624
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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