A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451262



Internal ID21108815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61661901..61666000hg38UCSC Ensembl
chr10:63421659..63425758hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183557
Samples
Known GenesC10orf107
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451262
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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