A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068084



Internal ID21977317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73573846..73573846hg38UCSC Ensembl
chr7:72988176..72988176hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574498
Samples
Known GenesTBL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068084
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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