A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438918



Internal ID21096471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23324592..23350487hg38UCSC Ensembl
chr10:23613521..23639416hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3825896
hg1925896
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179284
Samples
Known GenesC10orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438918
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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