A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15179278



Internal ID21318074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192641104..192641404hg38UCSC Ensembl
chr3:192358893..192359193hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3953657
Supporting Variants
SamplesHG002
Known GenesFGF12
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15179278
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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