A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325204



Internal ID20858335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:189026101..189994800hg38UCSC Ensembl
chr1:188995232..189963930hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38968700
hg19968699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv470n223
Supporting Variantsnssv18199165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325204
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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