A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152182



Internal ID21424252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95669183..95669183hg38UCSC Ensembl
chr6:96117059..96117059hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634508
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152182
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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