A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037441



Internal ID20604481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67966801..67969400hg38UCSC Ensembl
chr17:65962917..65965516hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526320
Supporting Variants
Samples
Known GenesBPTF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037441
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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