A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034895



Internal ID20601935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31466047..31469499hg38UCSC Ensembl
chr17:29793065..29796517hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg383453
hg193453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508644
Supporting Variants
Samples
Known GenesRAB11FIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034895
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