A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005470



Internal ID21914813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123809980..123810032hg38UCSC Ensembl
chr8:124822220..124822272hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578912
Samples
Known GenesFAM91A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005470
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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