A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403601



Internal ID22461471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96350471..96350471hg38UCSC Ensembl
chr1:96816027..96816027hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967386
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403601
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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