A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416209



Internal ID21073762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:14282881..14300225hg38UCSC Ensembl
chr8:14140390..14157734hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3817345
hg1917345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167378
Samples
Known GenesSGCZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416209
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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