A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16976827



Internal ID51937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177669324..177682000hg38UCSC Ensembl
chr5:177096325..177109001hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3812677
hg1912677
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141283
Supporting Variants
Samples
Known GenesLOC202181
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16976827
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000157


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