A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543098



Internal ID21867453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77917873..77923666hg38UCSC Ensembl
chr3:77967024..77972817hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg385794
hg195794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994709
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543098
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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