A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977915



Internal ID52676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181469324..181478200hg38UCSC Ensembl
chr5:180896325..180905201hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg388877
hg198877
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416998
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977915
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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