A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072128



Internal ID21457728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101506244..101506244hg38UCSC Ensembl
chr11:101376975..101376975hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650075
Supporting Variants
SamplesHG02587
Known GenesTRPC6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072128
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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