A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449498



Internal ID21107051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35630130..35642061hg38UCSC Ensembl
chr10:35919058..35930989hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3811932
hg1911932
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179890
Samples
Known GenesFZD8, MIR4683
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449498
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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