A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952933



Internal ID16955120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14984544..15030343hg38UCSC Ensembl
Outerchr16:15078401..15124200hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3845800
hg1945800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999233
SamplesBILGI_BIOE
Known GenesPDXDC1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952933
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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