A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141842



Internal ID21470880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160603284..160603284hg38UCSC Ensembl
chr6:161024316..161024316hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381405
hg191405
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635554
Supporting Variants
SamplesHG03125
Known GenesLPA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141842
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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