A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127774



Internal ID20694814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162665841..162670941hg38UCSC Ensembl
chr5:162092847..162097947hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg385101
hg195101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400947
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127774
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