A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975424



Internal ID22750359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47775210..47775210hg38UCSC Ensembl
chr11:47796762..47796762hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358375
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975424
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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