A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063302



Internal ID19152521
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 StatusM
Merged Variantsdgv2985n100
Supporting Variantsnssv3559305, nssv3559304, nssv3559301, nssv3559303, nssv3559302
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)nsv1063302
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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