A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929793



Internal ID22705052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53678272..53720859hg38UCSC Ensembl
chr17:51755633..51798220hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3842588
hg1942588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929793
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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