A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6245577



Internal ID22050187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169009740..169009740hg38UCSC Ensembl
chr1:168978978..168978978hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17839705
Samples
Known GenesLINC00970
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6245577
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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