A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067588



Internal ID21505951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121673768..121701904hg38UCSC Ensembl
chr10:123433282..123461418hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3828137
hg1928137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590400
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067588
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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