A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036888



Internal ID20603928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:54986415..54987832hg38UCSC Ensembl
chr17:53063776..53065193hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381418
hg191418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526817
Supporting Variants
Samples
Known GenesSTXBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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