A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247124



Internal ID22051734
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 StatusM
Merged Variants
Supporting Variantsnssv17841901
Samples
Known GenesANK3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247124
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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