A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918310



Internal ID22693531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130456989..130475716hg38UCSC Ensembl
chr10:132255253..132273980hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3818728
hg1918728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354128
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918310
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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