A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014482



Internal ID21923825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107770153..107770244hg38UCSC Ensembl
chr7:107410598..107410689hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567114
Samples
Known GenesSLC26A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014482
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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