A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656848



Internal ID21605153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17077752..17077752hg38UCSC Ensembl
chr17:16981066..16981066hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090034
SamplesHG02011
Known GenesMPRIP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656848
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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