A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575963



Internal ID21524397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95079883..95079935hg38UCSC Ensembl
chr8:96092111..96092163hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141347
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575963
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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