A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15261138



Internal ID4316926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60068271..60073153hg38UCSC Ensembl
Innerchr15:60068271..60073153hg38UCSC Ensembl
Outerchr15:60068240..60073283hg38UCSC Ensembl
chr15:60360470..60365352hg19UCSC Ensembl
Innerchr15:60360470..60365352hg19UCSC Ensembl
Outerchr15:60360439..60365482hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg384883
hg194883
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636653
Supporting Variants
SamplesHG03868
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15261138
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