A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664403



Internal ID21612708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64969421..64969421hg38UCSC Ensembl
chr17:62965539..62965539hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093865
SamplesHG03065
Known GenesAMZ2P1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664403
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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