A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088619



Internal ID21491441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7083650..7083830hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590176
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088619
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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