A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951410



Internal ID22726772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110062618..110062618hg38UCSC Ensembl
chr1:110605240..110605240hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364432
Samples
Known GenesALX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951410
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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