A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422039



Internal ID21079592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10751243..10800599hg38UCSC Ensembl
chr8:10608753..10658109hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3849357
hg1949357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162117
Samples
Known GenesPINX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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