A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426641



Internal ID21084194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144780113..144783154hg38UCSC Ensembl
chr8:146005498..146008539hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg383042
hg193042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165584
Samples
Known GenesZNF34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426641
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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