A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464509



Internal ID242387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4656870..4662205hg38UCSC Ensembl
chr6:4657104..4662439hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg385336
hg195336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979949
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464509
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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