A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952903



Internal ID16955090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:2423400..2476599hg38UCSC Ensembl
Outerchr16:2473401..2526600hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3853200
hg1953200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999199
SamplesBILGI_BIOE
Known GenesABCA17P, C16orf59, CCNF, MIR6767, MIR6768, NTN3, TBC1D24
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952903
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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