A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10415058



Internal ID2223160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15016319..15057663hg38UCSC Ensembl
Innerchr2:15016469..15057513hg38UCSC Ensembl
Outerchr2:15016169..15057813hg38UCSC Ensembl
chr2:15156443..15197787hg19UCSC Ensembl
Innerchr2:15156593..15197637hg19UCSC Ensembl
Outerchr2:15156293..15197937hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3841345
hg1941345
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3589903
Supporting Variants
SamplesHG01997
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10415058
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