A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087601



Internal ID21433936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88646304..88646304hg38UCSC Ensembl
chr16:88712712..88712712hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646575
Supporting Variants
SamplesHG00731
Known GenesCYBA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087601
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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