A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132671



Internal ID20699711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68432042..68440204hg38UCSC Ensembl
chr5:67727869..67736031hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg388163
hg198163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402069
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132671
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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