A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154906



Internal ID21456441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26536906..26536906hg38UCSC Ensembl
chr6:26537134..26537134hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5629739
Supporting Variants
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154906
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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