A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062975



Internal ID19152194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77984145..78036704hg38UCSC Ensembl
Innerchr16:78018042..78070601hg19UCSC Ensembl
Innerchr16:76575543..76628102hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3852560
hg1952560
hg1852560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3032n100
Supporting Variantsnssv3559675, nssv3719064
Samples
Known GenesCLEC3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062975
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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