A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079215



Internal ID21489944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31097161..31097221hg38UCSC Ensembl
chr12:31250095..31250155hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603775
Supporting Variants
SamplesNA19238
Known GenesDDX11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079215
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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