A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157238



Internal ID21441005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73976049..73976103hg38UCSC Ensembl
chr8:74888284..74888338hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569848
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157238
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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