A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087860



Internal ID21486490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34572599..34572599hg38UCSC Ensembl
chr16:46403044..46403044hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656027
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087860
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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