A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3551975



Internal ID18850256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32618616..33818870hg38UCSC Ensembl
Innerchr16:32629937..33621337hg19UCSC Ensembl
Innerchr16:32537438..33528838hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381200255
hg19991401
hg18991401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066152
Supporting Variants
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3551975
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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