A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16895735



Internal ID171317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212658794..212663951hg38UCSC Ensembl
chr1:212832136..212837293hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg385158
hg195158
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562131
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16895735
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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