A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850521



Internal ID22034164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77130414..77130414hg38UCSC Ensembl
chr18:74842370..74842370hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6242709
Supporting Variants
Samples
Known GenesMBP
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850521
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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