A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944492



Internal ID22719958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:22744028..22747989hg38UCSC Ensembl
chr17:22243355..22247316hg19UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg383962
hg193962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944492
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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