A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076439



Internal ID21415736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93420970..93427030hg38UCSC Ensembl
chr11:93154136..93160196hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386061
hg196061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592472
Supporting Variants
SamplesHG00731
Known GenesCCDC67
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076439
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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