A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035536



Internal ID20602576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4221901..4222500hg38UCSC Ensembl
chr17:4125196..4125795hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497232
Supporting Variants
Samples
Known GenesANKFY1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035536
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08461


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