A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039208



Internal ID20606248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81830201..81831600hg38UCSC Ensembl
chr17:79788077..79789476hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519230
Supporting Variants
Samples
Known GenesFAM195B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039208
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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