A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007129



Internal ID20574169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109959105..109959659hg38UCSC Ensembl
chr13:110611452..110612006hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480983
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0008


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