A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438196



Internal ID21095749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110297801..110308500hg38UCSC Ensembl
chr10:112057559..112068258hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195733
Samples
Known GenesSMNDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438196
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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