A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920971



Internal ID22696194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17475776..17476775hg38UCSC Ensembl
chr10:17517775..17518774hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920971
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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