A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977318



Internal ID52278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154897843..154897935hg38UCSC Ensembl
chr5:154277403..154277495hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473711
Supporting Variants
Samples
Known GenesGEMIN5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977318
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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