A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952955



Internal ID16955142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:23981380..23982679hg38UCSC Ensembl
Outerchr16:23992701..23994000hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000058
SamplesBILGI_BIOE
Known GenesPRKCB
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952955
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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