A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964996



Internal ID22739931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88930168..88930168hg38UCSC Ensembl
chr6:89639887..89639887hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439757
Samples
Known GenesRNGTT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964996
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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