A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839527



Internal ID22023170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157066807..157066807hg38UCSC Ensembl
chr7:156859501..156859501hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6239959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839527
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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