A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072442



Internal ID21414240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106710134..106710134hg38UCSC Ensembl
chr11:106580860..106580860hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649247
Supporting Variants
SamplesHG00513
Known GenesGUCY1A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072442
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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