A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093443



Internal ID21470211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81078518..81078518hg38UCSC Ensembl
chr17:79052318..79052318hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645331
Supporting Variants
SamplesHG03125
Known GenesBAIAP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093443
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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