A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448982



Internal ID21106535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132406401..132424871hg38UCSC Ensembl
chr10:134219905..134238375hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3818471
hg1918471
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183374
Samples
Known GenesPWWP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448982
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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