A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16974739



Internal ID50539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149477283..149478496hg38UCSC Ensembl
chr5:148856846..148858059hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381214
hg191214
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555824
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16974739
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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