A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929363



Internal ID22704615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63774486..63774538hg38UCSC Ensembl
chr17:61851846..61851898hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373303
Samples
Known GenesDDX42
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929363
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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