A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366781



Internal ID22592450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16032248..16046348hg38UCSC Ensembl
chr1:16358743..16372843hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3814101
hg1914101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867713
Supporting Variants
Samples
Known GenesCLCNKA, CLCNKB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366781
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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