A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952918



Internal ID16955105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:9092244..9122043hg38UCSC Ensembl
Outerchr16:9186101..9215900hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3829800
hg1929800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999215
SamplesBILGI_BIOE
Known GenesC16orf72
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952918
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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