A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925017



Internal ID22700244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15739393..15740942hg38UCSC Ensembl
chr10:15781392..15782941hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381550
hg191550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363881
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925017
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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