A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650995



Internal ID21599300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82764853..82764853hg38UCSC Ensembl
chr17:80722729..80722729hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099613
SamplesHG00732
Known GenesTBCD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650995
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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