A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001393



Internal ID16947659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:53220885..53236584hg38UCSC Ensembl
Outerchr3:53254901..53270600hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3815700
hg1915700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954864
Supporting Variants
SamplesBILGI_BIOE
Known GenesTKT
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001393
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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