A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859985



Internal ID22043628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30962343..30962343hg38UCSC Ensembl
chr7:31001958..31001958hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6261240
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859985
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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