A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442733



Internal ID21100286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87073702..87108378hg38UCSC Ensembl
chr10:88833459..88868135hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3834677
hg1934677
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197116
Samples
Known GenesFAM35A, GLUD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442733
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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