A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964138



Internal ID22739073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81721232..81721232hg38UCSC Ensembl
chr3:81770383..81770383hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415778
Samples
Known GenesGBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964138
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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