A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865357



Internal ID22640292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75082431..75084230hg38UCSC Ensembl
chr10:76842189..76843988hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460949
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865357
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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