A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600601



Internal ID21549242
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 StatusM
Merged Variants
Supporting Variantsnssv17115999
SamplesHG00731
Known GenesCOMMD7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600601
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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