A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16950656



Internal ID34456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70905767..70905818hg38UCSC Ensembl
chr4:71771484..71771535hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5413753
Supporting Variants
Samples
Known GenesMOB1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16950656
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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