A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331665



Internal ID20864830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:185276001..185277100hg38UCSC Ensembl
chr1:185245133..185246232hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054473
Samples
Known GenesSWT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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