A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334216



Internal ID20867399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207223714..207357241hg38UCSC Ensembl
chr1:207397059..207530586hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38133528
hg19133528
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199890
Samples
Known GenesCD55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334216
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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