A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372785



Internal ID22598454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67785731..67785731hg38UCSC Ensembl
chr16:67819634..67819634hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972362
Supporting Variants
Samples
Known GenesRANBP10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372785
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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