A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455432



Internal ID21112985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103962201..103974300hg38UCSC Ensembl
chr10:105721959..105734058hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3812100
hg1912100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194728
Samples
Known GenesSLK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455432
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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