A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452820



Internal ID21110373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87000010..87045517hg38UCSC Ensembl
chr10:88759767..88805274hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3845508
hg1945508
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190940
Samples
Known GenesAGAP11, FAM25A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452820
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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