A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466984



Internal ID244808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95596143..95611161hg38UCSC Ensembl
chr6:96044019..96059037hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3815019
hg1915019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985506
Samples
Known GenesMANEA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466984
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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