A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152887



Internal ID21460076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99550659..99550659hg38UCSC Ensembl
chr6:99998535..99998535hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635558
Supporting Variants
SamplesHG02818
Known GenesCCNC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152887
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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