A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450497



Internal ID21108050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32597923..32598970hg38UCSC Ensembl
chr10:32886851..32887898hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg381048
hg191048
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180438
Samples
Known GenesCCDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450497
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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