A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636958



Internal ID6677065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77200289..77219057hg38UCSC Ensembl
Innerchr15:77200292..77219055hg38UCSC Ensembl
Outerchr15:77200287..77219060hg38UCSC Ensembl
chr15:77492631..77511399hg19UCSC Ensembl
Innerchr15:77492634..77511397hg19UCSC Ensembl
Outerchr15:77492629..77511402hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3818769
hg1918769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15299960, essv15299959
SamplesHG02614, HG02574
Known GenesPEAK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636958
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