A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071767



Internal ID21981000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116534395..116534395hg38UCSC Ensembl
chr7:116174449..116174449hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570428
Samples
Known GenesCAV1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071767
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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