A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451688



Internal ID21109241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87019399..87067528hg38UCSC Ensembl
chr10:88779156..88827285hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3848130
hg1948130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195155
Samples
Known GenesFAM25A, GLUD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451688
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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