A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520837



Internal ID20894198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82834000..82840968hg38UCSC Ensembl
chr17:80791876..80798844hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg386969
hg196969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038350
Samples
Known GenesTBCD, ZNF750
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520837
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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