A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850032



Internal ID22624967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42888822..42891594hg38UCSC Ensembl
chr10:43384270..43387042hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382773
hg192773
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850032
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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