A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16899116



Internal ID182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244097520..244097530hg38UCSC Ensembl
chr1:244260822..244260832hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3811
hg1911
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563159
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16899116
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001561


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