A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16889235



Internal ID166917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151998626..152000241hg38UCSC Ensembl
chr1:151971102..151972717hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381616
hg191616
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555143
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16889235
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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