A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3550364



Internal ID18848645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32169453..32560003hg38UCSC Ensembl
Innerchr16:32180774..32571324hg19UCSC Ensembl
Innerchr16:32088275..32478825hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38390551
hg19390551
hg18390551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065967
Supporting Variants
Samples
Known GenesLOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3550364
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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