A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074936



Internal ID21502749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3961125..3961630hg38UCSC Ensembl
chr11:3982355..3982860hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587329
Supporting Variants
SamplesNA19239
Known GenesSTIM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074936
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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