A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116800



Internal ID21422136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50301101..50301197hg38UCSC Ensembl
chr20:48917638..48917734hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593716
Supporting Variants
SamplesHG00731
Known GenesLOC284751
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116800
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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