A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321899



Internal ID20855008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:187599901..187636100hg38UCSC Ensembl
chr1:187569033..187605232hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3836200
hg1936200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321899
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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