A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057284



Internal ID19146503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55755658..55782781hg38UCSC Ensembl
Innerchr16:55789570..55816693hg19UCSC Ensembl
Innerchr16:54347071..54374194hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3827124
hg1927124
hg1827124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2985n100
Supporting Variantsnssv3559300
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)nsv1057284
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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