A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850762



Internal ID22034405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39104531..39104531hg38UCSC Ensembl
chr1:39570203..39570203hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6252137
Supporting Variants
Samples
Known GenesMACF1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850762
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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