A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060866



Internal ID21482082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11829529..11829529hg38UCSC Ensembl
chr1:11889586..11889586hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610574
Supporting Variants
SamplesHG03683
Known GenesCLCN6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060866
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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