A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086890



Internal ID21502548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91293279..91293540hg38UCSC Ensembl
chr14:91759623..91759884hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599481
Supporting Variants
SamplesNA19239
Known GenesCCDC88C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086890
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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