A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036838



Internal ID20603878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51072427..51075680hg38UCSC Ensembl
chr17:49149788..49153041hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg383254
hg193254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534956
Supporting Variants
Samples
Known GenesSPAG9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036838
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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