A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970392



Internal ID47588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93559232..93560019hg38UCSC Ensembl
chr5:92894938..92895725hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38788
hg19788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458581
Supporting Variants
Samples
Known GenesNR2F1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970392
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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