A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430822



Internal ID21088375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13985293..14118174hg38UCSC Ensembl
chr8:13842802..13975683hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38132882
hg19132882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166590
Samples
Known GenesSGCZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430822
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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