A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005620



Internal ID21914963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14303818..14326545hg38UCSC Ensembl
chr7:14343443..14366170hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3822728
hg1922728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557652
Samples
Known GenesDGKB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005620
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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