A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277868



Internal ID20487086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144824437..144824437hg38UCSC Ensembl
chr6:145145573..145145573hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751433
Supporting Variants
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277868
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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