A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854740



Internal ID22038383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157572984..157572984hg38UCSC Ensembl
chr4:158494136..158494136hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6255575
Supporting Variants
Samples
Known GenesLOC340017
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854740
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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