A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633047



Internal ID21581352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2773769..2773769hg38UCSC Ensembl
chr6:2774003..2774003hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146580
SamplesHG00512
Known GenesWRNIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633047
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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