A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128791



Internal ID21416629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68418418..68418468hg38UCSC Ensembl
chr3:68467568..68467618hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568697
Supporting Variants
SamplesHG00731
Known GenesFAM19A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128791
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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