A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961084



Internal ID22736044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90870999..90870999hg38UCSC Ensembl
chr8:91883227..91883227hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435832
Samples
Known GenesNECAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961084
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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