A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073272



Internal ID21437567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131865893..131865893hg38UCSC Ensembl
chr11:131735787..131735787hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645134
Supporting Variants
SamplesHG00731
Known GenesNTM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073272
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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