A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901894



Internal ID2060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46782927..46791855hg38UCSC Ensembl
chr1:47248599..47257527hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg388929
hg198929
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560346
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901894
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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