A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117795



Internal ID21463644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63960306..63960686hg38UCSC Ensembl
chr20:62591659..62592039hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601983
Supporting Variants
SamplesHG03009
Known GenesZNF512B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117795
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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