A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035517



Internal ID20602557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41855796..41856116hg38UCSC Ensembl
chr17:40012048..40012368hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511105
Supporting Variants
Samples
Known GenesKLHL11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035517
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