A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958273



Internal ID22733347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99550659..99550659hg38UCSC Ensembl
chr6:99998535..99998535hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430524
Samples
Known GenesCCNC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958273
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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