A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029812



Internal ID87585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10736..10767hg38UCSC Ensembl
chr18:10932..10963hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546769
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029812
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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