A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052580



Internal ID20619620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:163339486..163340272hg38UCSC Ensembl
chr1:163309276..163310062hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38787
hg19787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331678
Supporting Variants
Samples
Known GenesNUF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052580
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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