A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154025



Internal ID21504003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35159022..35159022hg38UCSC Ensembl
chr6:35126799..35126799hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628722
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154025
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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