A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118927



Internal ID21414778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37717340..37717389hg38UCSC Ensembl
chr21:39089643..39089692hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594812
Supporting Variants
SamplesHG00513
Known GenesKCNJ6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118927
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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