A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606083



Internal ID21798130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87961680..87961680hg38UCSC Ensembl
chr14:88428024..88428024hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081963
Supporting Variants
Samples
Known GenesGALC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606083
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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