A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556034



Internal ID21880389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143012548..143012548hg38UCSC Ensembl
chr5:142392113..142392113hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076619
Supporting Variants
Samples
Known GenesARHGAP26
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556034
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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