A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420965



Internal ID22478835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11210766..11210766hg38UCSC Ensembl
chr6:11210999..11210999hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5960575
Supporting Variants
Samples
Known GenesNEDD9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420965
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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