A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139777



Internal ID21451580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41633817..41633817hg38UCSC Ensembl
chr6:41601555..41601555hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625109
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139777
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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