A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977678



Internal ID52506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177869112..177882100hg38UCSC Ensembl
chr5:177296113..177309101hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3812989
hg1912989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140697
Supporting Variants
Samples
Known GenesLOC728554
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977678
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.148508


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