A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074458



Internal ID21405743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:375140..375140hg38UCSC Ensembl
chr11:375140..375140hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652853
Supporting Variants
SamplesHG00512
Known GenesB4GALNT4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074458
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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