A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038661



Internal ID20605701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80022626..80034403hg38UCSC Ensembl
chr17:77996425..78008202hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3811778
hg1911778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519600
Supporting Variants
Samples
Known GenesTBC1D16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038661
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