A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453630



Internal ID21111183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99534901..99536400hg38UCSC Ensembl
chr10:101294658..101296157hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184156
Samples
Known GenesNKX2-3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453630
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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