A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116606



Internal ID21422218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52167425..52167492hg38UCSC Ensembl
chr20:50783964..50784031hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593315
Supporting Variants
SamplesHG00731
Known GenesZFP64
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116606
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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