A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3550412



Internal ID18848693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32197413..33970586hg38UCSC Ensembl
Innerchr16:32208734..33773053hg19UCSC Ensembl
Innerchr16:32116235..33680554hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381773174
hg191564320
hg181564320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066639
Supporting Variants
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3550412
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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