A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071546



Internal ID21436823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9273065..9273261hg38UCSC Ensembl
chr10:9315028..9315224hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585931
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071546
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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