A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551914



Internal ID21876269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143424719..143424719hg38UCSC Ensembl
chr5:142804284..142804284hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg381771
hg191771
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079408
Supporting Variants
Samples
Known GenesNR3C1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551914
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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