A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3542854



Internal ID18841135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19932666..19958920hg38UCSC Ensembl
Innerchr16:19943988..19970242hg19UCSC Ensembl
Innerchr16:19851489..19877743hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3826255
hg1926255
hg1826255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038864
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)nssv3542854
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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