A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000069



Internal ID17293021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:29283980..29315979hg38UCSC Ensembl
Outerchr16:29295301..29327300hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3832000
hg1932000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952965
Supporting Variants
SamplesBILGI_BIOE
Known GenesSNX29P2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000069
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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