A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437036



Internal ID21094589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32385803..32626568hg38UCSC Ensembl
chr10:32674731..32915496hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38240766
hg19240766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193519
Samples
Known GenesCCDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437036
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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