A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952928



Internal ID16955115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14719144..14745243hg38UCSC Ensembl
Outerchr16:14813001..14839100hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3826100
hg1926100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999226
SamplesBILGI_BIOE
Known GenesNPIPA2, NPIPA3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952928
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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