A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004101



Internal ID70369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108911153..108911153hg38UCSC Ensembl
chr7:108551210..108551210hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5411978
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004101
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.037705


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