A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892949



Internal ID169464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178017216..178017267hg38UCSC Ensembl
chr1:177986351..177986402hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5396694
Supporting Variants
Samples
Known GenesLOC730102
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892949
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.006556


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