A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900529



Internal ID1142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:731650..915000hg38UCSC Ensembl
chr1:667030..850380hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38183351
hg19183351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422961
Supporting Variants
Samples
Known GenesFAM41C, FAM87B, LINC00115, LINC01128, LOC100288069
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900529
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01542


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