A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645331



Internal ID21593636
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 StatusM
Merged Variants
Supporting Variantsnssv17093443
SamplesHG03125
Known GenesBAIAP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645331
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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