A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324008



Internal ID20857131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209883901..209904700hg38UCSC Ensembl
chr1:210057246..210078045hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3820800
hg1920800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199921
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324008
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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