A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423239



Internal ID21080792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91395401..91398700hg38UCSC Ensembl
chr8:92407629..92410928hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7421n223
Supporting Variantsnssv18172781
Samples
Known GenesSLC26A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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