A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067163



Internal ID21976396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2893212..2893212hg38UCSC Ensembl
chr6:2893446..2893446hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557988
Samples
Known GenesSERPINB9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067163
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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