A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950306



Internal ID17299180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:195851430..195893129hg38UCSC Ensembl
Outerchr3:195578301..195620000hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3841700
hg1941700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996597
SamplesBILGI_BIOE
Known GenesMIR6829, TNK2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950306
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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