A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968503



Internal ID46319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77885702..77886925hg38UCSC Ensembl
chr5:77181526..77182749hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381224
hg191224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459813
Supporting Variants
Samples
Known GenesLOC101929154
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968503
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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