A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005643



Internal ID16951909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:3868289..3868485hg38UCSC Ensembl
Outerchr16:3918290..3918486hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958207
Supporting Variants
SamplesBILGI_BIOE
Known GenesCREBBP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005643
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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