A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041481



Internal ID18784012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15886652..15930167hg38UCSC Ensembl
Innerchr16:15980509..16024024hg19UCSC Ensembl
Innerchr16:15888010..15931525hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3843516
hg1943516
hg1843516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2774n100
Supporting Variantsnssv3557981, nssv3557980
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)nsv1041481
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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