A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005938



Internal ID71572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155786284..155786335hg38UCSC Ensembl
chr7:155578978..155579029hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5413225
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005938
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001873


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