A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015092



Internal ID21924435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91394097..91394393hg38UCSC Ensembl
chr8:92406325..92406621hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592396
Samples
Known GenesSLC26A7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015092
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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