A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3556998



Internal ID18508593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5328428..5387609hg38UCSC Ensembl
Innerchr16:5378429..5437610hg19UCSC Ensembl
Innerchr16:5318430..5377611hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3859182
hg1959182
hg1859182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052903
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3556998
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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