A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334603



Internal ID20867790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224165911..224167097hg38UCSC Ensembl
chr1:224353613..224354799hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg381187
hg191187
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334603
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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