A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267907



Internal ID20477125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128731741..128731889hg38UCSC Ensembl
chr3:128450584..128450732hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743433
Supporting Variants
Samples
Known GenesRAB7A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267907
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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