A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955465



Internal ID22730665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39888757..39888757hg38UCSC Ensembl
chr1:40354429..40354429hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955465
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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