A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429834



Internal ID21087387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10728947..10740687hg38UCSC Ensembl
chr8:10586457..10598197hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3811741
hg1911741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162094
Samples
Known GenesSOX7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429834
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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