A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120403



Internal ID21439275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99886216..99886268hg38UCSC Ensembl
chr3:99605060..99605112hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567725
Supporting Variants
SamplesHG00732
Known GenesCMSS1, FILIP1L, MIR548G
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120403
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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