A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956480



Internal ID22731666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74753816..74753816hg38UCSC Ensembl
chr10:76513574..76513574hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363185
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956480
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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