A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434655



Internal ID22492525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40042280..40042280hg38UCSC Ensembl
chr8:39899799..39899799hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5950473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434655
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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