A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16899119



Internal ID185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244108281..244108407hg38UCSC Ensembl
chr1:244271583..244271709hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557371
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16899119
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000624


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