A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654698



Internal ID21603003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81056794..81056794hg38UCSC Ensembl
chr17:79030594..79030594hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081902, nssv17083838
SamplesHG00731, HG00732
Known GenesBAIAP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654698
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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