A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920992



Internal ID22696215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101576264..101579708hg38UCSC Ensembl
chr10:103336021..103339465hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg383445
hg193445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361014
Samples
Known GenesPOLL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920992
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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