A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424177



Internal ID21081730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122869885..122880566hg38UCSC Ensembl
chr8:123882124..123892805hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3810682
hg1910682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163993
Samples
Known GenesZHX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424177
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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