A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956255



Internal ID16958443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:191346879..191353837hg38UCSC Ensembl
Outerchr3:191064668..191071626hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg386959
hg196959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv132n73
Supporting Variantsnssv3004451
SamplesBILGI_BIOE
Known GenesCCDC50
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956255
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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