A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415770



Internal ID21073323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122836160..122840427hg38UCSC Ensembl
chr8:123848399..123852666hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg384268
hg194268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163991
Samples
Known GenesZHX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415770
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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