A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16924038



Internal ID16781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:128285186..129050431hg38UCSC Ensembl
chr2:129042760..129808004hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg38765246
hg19765245
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557549
Supporting Variants
Samples
Known GenesHS6ST1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16924038
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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