A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090156



Internal ID21432774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64738107..64738107hg38UCSC Ensembl
chr16:64772010..64772010hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655092
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090156
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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