A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17838686



Internal ID22022329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64849522..64849522hg38UCSC Ensembl
chr7:64309900..64309900hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257457
Supporting Variants
Samples
Known GenesZNF138
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17838686
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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