A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257245



Internal ID22061855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137359734..137359734hg38UCSC Ensembl
chr6:137680871..137680871hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17860053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257245
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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