A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330783



Internal ID20863941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206963894..207016277hg38UCSC Ensembl
chr1:207137239..207189622hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3852384
hg1952384
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199888
Samples
Known GenesFCAMR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330783
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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