A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256630



Internal ID22061240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8281629..8281629hg38UCSC Ensembl
chr6:8281862..8281862hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17858745
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256630
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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