A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039156



Internal ID20606196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9578303..9586331hg38UCSC Ensembl
chr17:9481620..9489648hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg388029
hg198029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499493
Supporting Variants
Samples
Known GenesWDR16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039156
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