A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069807



Internal ID21481523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35491857..35491906hg38UCSC Ensembl
chr10:35780785..35780834hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591829
Supporting Variants
SamplesHG03683
Known GenesCCNY
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069807
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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