A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652523



Internal ID21600828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75139819..75139819hg38UCSC Ensembl
chr17:73135914..73135914hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079891
SamplesHG03486
Known GenesHN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652523
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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