A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437484



Internal ID21095037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121597101..121599300hg38UCSC Ensembl
chr10:123356615..123358814hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179038
Samples
Known GenesFGFR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437484
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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