A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952920



Internal ID16955107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:11155244..11192743hg38UCSC Ensembl
Outerchr16:11249101..11286600hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3837500
hg1937500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999218
SamplesBILGI_BIOE
Known GenesCLEC16A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952920
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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