A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081902



Internal ID21442664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81056794..81056794hg38UCSC Ensembl
chr17:79030594..79030594hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654698
Supporting Variants
SamplesHG00732
Known GenesBAIAP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081902
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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