A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075046



Internal ID21438400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47557553..47557553hg38UCSC Ensembl
chr11:47579105..47579105hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655548
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075046
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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