A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318953



Internal ID20852045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207340001..207382400hg38UCSC Ensembl
chr1:207513346..207555745hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3842400
hg1942400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199891
Samples
Known GenesCD55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318953
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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