A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326189



Internal ID20859323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9554537..9555765hg38UCSC Ensembl
chr1:9614595..9615823hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381229
hg191229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066138
Samples
Known GenesSLC25A33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326189
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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