A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152298



Internal ID21405723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52940230..52940230hg38UCSC Ensembl
chr6:52805028..52805028hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643999
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152298
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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