A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3004699



Internal ID16950965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:101039003..101040052hg38UCSC Ensembl
Outerchr4:101960160..101961209hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381050
hg191050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv956313
Supporting Variants
SamplesBILGI_BIOE
Known GenesPPP3CA
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3004699
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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