A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453375



Internal ID21110928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126387501..126389700hg38UCSC Ensembl
chr10:128076070..128078269hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196001
Samples
Known GenesADAM12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453375
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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