A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461909



Internal ID239852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89443530..89453551hg38UCSC Ensembl
chr6:90153249..90163270hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3810022
hg1910022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985362
Samples
Known GenesANKRD6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461909
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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