A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068575



Internal ID21435633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11885356..11885472hg38UCSC Ensembl
chr10:11927355..11927471hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593551
Supporting Variants
SamplesHG00731
Known GenesPROSER2-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068575
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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