A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417677



Internal ID21075230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27925399..27927301hg38UCSC Ensembl
chr8:27782916..27784818hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg381903
hg191903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166133
Samples
Known GenesSCARA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417677
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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