A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048188



Internal ID18790719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15874385..15911711hg38UCSC Ensembl
Innerchr16:15968242..16005568hg19UCSC Ensembl
Innerchr16:15875743..15913069hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3837327
hg1937327
hg1837327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557974
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)nsv1048188
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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