A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075636



Internal ID21984869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:130424995..130424995hg38UCSC Ensembl
chr8:131437241..131437241hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg382316
hg192316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597240
Samples
Known GenesASAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075636
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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