A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045194



Internal ID18787725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15886652..15911711hg38UCSC Ensembl
Innerchr16:15980509..16005568hg19UCSC Ensembl
Innerchr16:15888010..15913069hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3825060
hg1925060
hg1825060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557975
Samples
Known GenesFOPNL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045194
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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