A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454798



Internal ID21112351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32639888..32655273hg38UCSC Ensembl
chr10:32928816..32944201hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3815386
hg1915386
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194456
Samples
Known GenesCCDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454798
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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