A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967222



Internal ID45460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78448345..78448396hg38UCSC Ensembl
chr5:77744169..77744220hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5404716
Supporting Variants
Samples
Known GenesSCAMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967222
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007649


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