A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371191



Internal ID22596860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5730842..5730842hg38UCSC Ensembl
chr18:5730841..5730841hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970036
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371191
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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