A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704770



Internal ID21377046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136950972..136951025hg38UCSC Ensembl
chr9:139845424..139845477hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389201
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704770
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0344828


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