A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17838752



Internal ID22022395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107584221..107584221hg38UCSC Ensembl
chr7:107224666..107224666hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6239551
Supporting Variants
Samples
Known GenesBCAP29
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17838752
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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