A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636274



Internal ID7023070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42520475..42525596hg38UCSC Ensembl
Innerchr15:42520975..42525096hg38UCSC Ensembl
Outerchr15:42519475..42526596hg38UCSC Ensembl
chr15:42812673..42817794hg19UCSC Ensembl
Innerchr15:42813173..42817294hg19UCSC Ensembl
Outerchr15:42811673..42818794hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg385122
hg195122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15231051
SamplesHG04202
Known GenesSNAP23
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636274
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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