A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078784



Internal ID21988017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1047614..1047614hg38UCSC Ensembl
chr7:1087250..1087250hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558771
Samples
Known GenesC7orf50
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078784
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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