A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074307



Internal ID21465700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2379375..2379436hg38UCSC Ensembl
chr11:2400605..2400666hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590726
Supporting Variants
SamplesHG03065
Known GenesCD81
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074307
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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