A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435148



Internal ID21092701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91395701..91398800hg38UCSC Ensembl
chr8:92407929..92411028hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7421n223
Supporting Variantsnssv18172783
Samples
Known GenesSLC26A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435148
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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