A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151568



Internal ID21451748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27876745..27876745hg38UCSC Ensembl
chr6:27844523..27844523hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624730
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151568
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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