A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072806



Internal ID21982039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161382536..161382536hg38UCSC Ensembl
chr5:160809542..160809542hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382423
hg192423
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573973
Samples
Known GenesGABRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072806
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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