A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862684



Internal ID22637619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87123492..87141738hg38UCSC Ensembl
chr10:88883249..88901495hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3818247
hg1918247
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466440
Samples
Known GenesFAM35A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862684
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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