A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034016



Internal ID20601056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10322361..10323684hg38UCSC Ensembl
chr17:10225678..10227001hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381324
hg191324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505277
Supporting Variants
Samples
Known GenesMYH13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034016
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