A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036136



Internal ID20603176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49671988..49673340hg38UCSC Ensembl
chr17:47749350..47750702hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg381353
hg191353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515802
Supporting Variants
Samples
Known GenesSPOP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036136
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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