A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559974



Internal ID18858255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86518894..86545426hg38UCSC Ensembl
Innerchr16:86552500..86579032hg19UCSC Ensembl
Innerchr16:85110001..85136533hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3826533
hg1926533
hg1826533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059266
Supporting Variants
Samples
Known GenesMTHFSD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559974
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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