A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331464



Internal ID20864627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33391285..33408255hg38UCSC Ensembl
chr1:33856886..33873856hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3816971
hg1916971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331464
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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