A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967306



Internal ID22742241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77654724..77654724hg38UCSC Ensembl
chr2:77881850..77881850hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391496
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967306
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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