A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841901



Internal ID22025544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60295773..60295773hg38UCSC Ensembl
chr10:62055531..62055531hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6247124
Supporting Variants
Samples
Known GenesANK3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841901
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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