A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968162



Internal ID46088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61664252..61664335hg38UCSC Ensembl
chr5:60960079..60960162hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472802
Supporting Variants
Samples
Known GenesC5orf64
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968162
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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