A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16895255



Internal ID171016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205952377..205953044hg38UCSC Ensembl
chr1:205921505..205922172hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560030
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16895255
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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