A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128021



Internal ID21509855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186071683..186072092hg38UCSC Ensembl
chr3:185789472..185789881hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572028
Supporting Variants
SamplesNA20847
Known GenesETV5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128021
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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