A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17853026



Internal ID22036669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7410786..7410786hg38UCSC Ensembl
chr1:7470846..7470846hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6252890
Supporting Variants
Samples
Known GenesCAMTA1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17853026
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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