A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145839



Internal ID21421523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40118542..40118631hg38UCSC Ensembl
chr8:39976061..39976150hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574904
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145839
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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