A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16974411



Internal ID50311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:136086262..136093689hg38UCSC Ensembl
chr5:135421951..135429378hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg387428
hg197428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470525
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16974411
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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