A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16914625



Internal ID10494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67334164..67334382hg38UCSC Ensembl
chr2:67561296..67561514hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560109
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16914625
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.030909


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