A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364940



Internal ID22590609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64553153..64553153hg38UCSC Ensembl
chr11:64320625..64320625hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969570
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364940
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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