A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012182



Internal ID21921525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107685939..107686155hg38UCSC Ensembl
chr7:107326384..107326600hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558296
Samples
Known GenesSLC26A4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012182
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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