A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608536



Internal ID21800583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92719237..92719293hg38UCSC Ensembl
chr14:93185582..93185638hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030968
Supporting Variants
Samples
Known GenesLGMN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608536
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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