A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038346



Internal ID20605386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8278673..8303809hg38UCSC Ensembl
chr17:8181991..8207127hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3825137
hg1925137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496736
Supporting Variants
Samples
Known GenesRANGRF, SLC25A35
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038346
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