A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656492



Internal ID21604797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64678063..64678063hg38UCSC Ensembl
chr17:62674181..62674181hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081001
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656492
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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