A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075882



Internal ID21439014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75004346..75004346hg38UCSC Ensembl
chr11:74715391..74715391hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381936
hg191936
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663502
Supporting Variants
SamplesHG00732
Known GenesNEU3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075882
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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