A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891396



Internal ID22666434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96887902..96891733hg38UCSC Ensembl
chr6:97335778..97339609hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg383832
hg193832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437752
Samples
Known GenesNDUFAF4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891396
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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