A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977464



Internal ID52376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161369686..161369996hg38UCSC Ensembl
chr5:160796692..160797002hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466701
Supporting Variants
Samples
Known GenesGABRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977464
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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