A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851663



Internal ID22626598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126671611..126672877hg38UCSC Ensembl
chr10:128360180..128361446hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg381267
hg191267
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468748, nssv17463515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851663
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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