A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088041



Internal ID21484697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64967111..64967111hg38UCSC Ensembl
chr17:62963229..62963229hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655392
Supporting Variants
SamplesNA12329
Known GenesAMZ2P1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088041
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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