A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144819



Internal ID21455841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56536216..56536216hg38UCSC Ensembl
chr6:56401014..56401014hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg381098
hg191098
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640386
Supporting Variants
SamplesHG02492
Known GenesDST, RNU6-71P
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144819
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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