A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380373



Internal ID22438243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69709861..69709861hg38UCSC Ensembl
chr1:70175544..70175544hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954240
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380373
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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