A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958705



Internal ID22733767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47962671..47962671hg38UCSC Ensembl
chr10:47127765..47127765hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367509
Samples
Known GenesLINC00842
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958705
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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