A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918377



Internal ID22693598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17144798..17145139hg38UCSC Ensembl
chr9:17144796..17145137hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436577
Samples
Known GenesCNTLN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918377
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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