A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980264



Internal ID22755199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16353372..16353372hg38UCSC Ensembl
chr17:16256686..16256686hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385700
Samples
Known GenesCENPV
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980264
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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