A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033290



Internal ID20600330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13515407..13519354hg38UCSC Ensembl
chr17:13418724..13422671hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg383948
hg193948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507382
Supporting Variants
Samples
Known GenesHS3ST3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033290
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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