A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051901



Internal ID20618941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117966313..117970240hg38UCSC Ensembl
chr1:118508936..118512863hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg383928
hg193928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331200
Supporting Variants
Samples
Known GenesSPAG17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051901
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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