A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115999



Internal ID21422520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32739555..32740226hg38UCSC Ensembl
chr20:31327362..31328033hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600601
Supporting Variants
SamplesHG00731
Known GenesCOMMD7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115999
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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