A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952959



Internal ID16955146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:27211480..27233779hg38UCSC Ensembl
Outerchr16:27222801..27245100hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3822300
hg1922300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000062
SamplesBILGI_BIOE
Known GenesKDM8, NSMCE1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952959
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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