A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17856181



Internal ID22039824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77021552..77021552hg38UCSC Ensembl
chr4:77942705..77942705hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254864
Supporting Variants
Samples
Known GenesSEPT11
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17856181
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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