A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965361



Internal ID22740296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173917605..173917605hg38UCSC Ensembl
chr1:173886743..173886743hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360785
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965361
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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