A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963043



Internal ID22737978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28247158..28247158hg38UCSC Ensembl
chr1:28573669..28573669hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963043
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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