A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964695



Internal ID22739630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59014494..59014494hg38UCSC Ensembl
chr1:59480166..59480166hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374695
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964695
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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