A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186273



Internal ID20753314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41422708..41439319hg38UCSC Ensembl
chr17:39578960..39595571hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3816612
hg1916612
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498137
Supporting Variants
Samples
Known GenesKRT37, KRT38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186273
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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