A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162384



Internal ID21428617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63976176..63976496hg38UCSC Ensembl
chrUn_gl000211:7739..8049hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38321
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588261
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162384
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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