A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155826



Internal ID21425819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:62017584..62017895hg38UCSC Ensembl
chr8:62930143..62930454hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567270
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155826
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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