A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955844



Internal ID22731040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63507644..63507644hg38UCSC Ensembl
chr10:65267404..65267404hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955844
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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