A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953806



Internal ID17302680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:31701480..31709379hg38UCSC Ensembl
Outerchr16:31712801..31720700hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000079
SamplesBILGI_BIOE
Known GenesCLUHP3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953806
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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