A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438441



Internal ID21095994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124839837..124870627hg38UCSC Ensembl
chr10:126528406..126559196hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3830791
hg1930791
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183541
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438441
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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