A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155817



Internal ID21462248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100979464..100979464hg38UCSC Ensembl
chr6:101427340..101427340hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627442
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155817
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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