A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964522



Internal ID22739457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180859067..180859067hg38UCSC Ensembl
chr1:180828203..180828203hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351526
Samples
Known GenesXPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964522
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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