A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649746



Internal ID21598051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76378386..76378386hg38UCSC Ensembl
chr17:74374467..74374467hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081338
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649746
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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