A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6243963



Internal ID22048573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36767997..36767997hg38UCSC Ensembl
chr4:36769619..36769619hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17853724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6243963
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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