A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038350



Internal ID20605390
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 StatusS
Merged Variantsnsv6520837
Supporting Variants
Samples
Known GenesTBCD, ZNF750
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038350
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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