A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428290



Internal ID21085843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144784954..144786737hg38UCSC Ensembl
chr8:146010339..146012122hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg381784
hg191784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165586
Samples
Known GenesZNF34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428290
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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