A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718827



Internal ID19017108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:881686..966057hg38UCSC Ensembl
Innerchr16:931686..1016057hg19UCSC Ensembl
Innerchr16:871687..956058hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3884372
hg1984372
hg1884372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042868
Supporting Variants
Samples
Known GenesLMF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718827
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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