A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547692



Internal ID21872047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:124170037..124170862hg38UCSC Ensembl
chr3:123888884..123889709hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991237
Supporting Variants
Samples
Known GenesKALRN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547692
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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