A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956021



Internal ID22731214
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 Variantsnssv17434389
Samples
Known GenesWRNIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956021
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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