A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149849



Internal ID21452295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41639230..41639230hg38UCSC Ensembl
chr6:41606968..41606968hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381498
hg191498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640336
Supporting Variants
SamplesHG01596
Known GenesMDFI
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149849
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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