A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17838362



Internal ID22022005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91202612..91202612hg38UCSC Ensembl
chr7:90831927..90831927hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257475
Supporting Variants
Samples
Known GenesCDK14
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17838362
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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