A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17859920



Internal ID22043563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:156023712..156023712hg38UCSC Ensembl
chr6:156344846..156344846hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17859920
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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