A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070317



Internal ID21504444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50675746..50676476hg38UCSC Ensembl
chr10:52435506..52436236hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590957
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070317
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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