A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927249



Internal ID18880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173171840..173171891hg38UCSC Ensembl
chr2:174036568..174036619hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5394883
Supporting Variants
Samples
Known GenesZAK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927249
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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