A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559301



Internal ID18857582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55755658..55788045hg38UCSC Ensembl
Innerchr16:55789570..55821957hg19UCSC Ensembl
Innerchr16:54347071..54379458hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3832388
hg1932388
hg1832388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063302
Supporting Variants
Samples
Known GenesCES1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559301
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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