A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751819



Internal ID21386299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96606359..96607413hg38UCSC Ensembl
chr9:99368641..99369695hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381055
hg191055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435799
Supporting Variants
SamplesMDQ010
Known GenesCDC14B
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751819
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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