A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065976



Internal ID19155195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55756974..55788045hg38UCSC Ensembl
Innerchr16:55790886..55821957hg19UCSC Ensembl
Innerchr16:54348387..54379458hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3831072
hg1931072
hg1831072
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559308, nssv3559307
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)nsv1065976
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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