A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023624



Internal ID20590664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34222940..34223861hg38UCSC Ensembl
chr15:34515141..34516062hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38922
hg19922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499320
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023624
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00025


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