A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035417



Internal ID20602457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30793961..30794384hg38UCSC Ensembl
chr17:29120979..29121402hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515221
Supporting Variants
Samples
Known GenesCRLF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00017


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