A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637058



Internal ID6677165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82590287..82726611hg38UCSC Ensembl
chr15:83259037..83395363hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38136325
hg19136327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15309993
SamplesHG03796
Known GenesAP3B2, CPEB1, LOC283692, LOC283693, LOC338963
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637058
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