A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333766



Internal ID20866947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9541101..9542100hg38UCSC Ensembl
chr1:9601160..9602159hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066122
Samples
Known GenesSLC25A33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333766
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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