A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174063



Internal ID20741103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129492313..129495256hg38UCSC Ensembl
chr9:132254592..132257535hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382944
hg192944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452143
Supporting Variants
Samples
Known GenesLINC00963
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174063
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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