A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977737



Internal ID52549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178179176..178181695hg38UCSC Ensembl
chr5:177606177..177608696hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg382520
hg192520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470759
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977737
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.006573


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