A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952900



Internal ID16955087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:1724500..1827999hg38UCSC Ensembl
Outerchr16:1774501..1878000hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38103500
hg19103500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999196
SamplesBILGI_BIOE
Known GenesEME2, FAHD1, HAGH, IGFALS, MAPK8IP3, MIR3177, MRPS34, NME3, NUBP2, SPSB3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952900
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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