A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416371



Internal ID21073924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123248302..123248909hg38UCSC Ensembl
chr8:124260542..124261149hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164007
Samples
Known GenesZHX1, ZHX1-C8ORF76
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416371
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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