A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446437



Internal ID22504307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81852217..81852217hg38UCSC Ensembl
chr7:81481533..81481533hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961699
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446437
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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