A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17839326



Internal ID22022969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140476573..140476573hg38UCSC Ensembl
chr7:140176373..140176373hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6239837
Supporting Variants
Samples
Known GenesMKRN1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17839326
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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