A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452134



Internal ID21109687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126386601..126388900hg38UCSC Ensembl
chr10:128075170..128077469hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190221
Samples
Known GenesADAM12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452134
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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