A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076512



Internal ID21985745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107686316..107686316hg38UCSC Ensembl
chr7:107326761..107326761hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562934
Samples
Known GenesSLC26A4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076512
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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