A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332708



Internal ID20865882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193102301..193108600hg38UCSC Ensembl
chr1:193071431..193077730hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199845
Samples
Known GenesGLRX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332708
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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