A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858577



Internal ID22633512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45792280..45807440hg38UCSC Ensembl
chr10:46287728..46302888hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3815161
hg1915161
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455755
Samples
Known GenesFAM21C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858577
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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