A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426571



Internal ID21084124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:14285973..14286467hg38UCSC Ensembl
chr8:14143482..14143976hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167380
Samples
Known GenesSGCZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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