A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292967



Internal ID20502185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137908251..137908422hg38UCSC Ensembl
chr9:140802703..140802874hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737947
Supporting Variants
Samples
Known GenesCACNA1B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292967
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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