A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975956



Internal ID51369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157566094..157566127hg38UCSC Ensembl
chr5:156993102..156993135hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3834
hg1934
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558591
Supporting Variants
Samples
Known GenesADAM19
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975956
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.003122


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