A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154369



Internal ID21425215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73695361..73695447hg38UCSC Ensembl
chr8:74607596..74607682hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575088
Supporting Variants
SamplesHG00731
Known GenesSTAU2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154369
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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