A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963071



Internal ID22738006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9008048..9008048hg38UCSC Ensembl
chr10:9050011..9050011hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963071
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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