A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953800



Internal ID16955987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:29804780..29816179hg38UCSC Ensembl
Outerchr16:29816101..29827500hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3811400
hg1911400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000072
SamplesBILGI_BIOE
Known GenesKIF22, MAZ, PRRT2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953800
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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