A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17349748



Internal ID22526726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119010728..119010728hg38UCSC Ensembl
chr1:119553351..119553351hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17349748
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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