A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959231



Internal ID22734270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104741700..104741700hg38UCSC Ensembl
chr10:106501458..106501458hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365556
Samples
Known GenesSORCS3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959231
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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