A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158377



Internal ID21472234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137810243..137810243hg38UCSC Ensembl
chr6:138131380..138131380hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642755
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158377
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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