A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3549138



Internal ID18500733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27185572..27224774hg38UCSC Ensembl
Innerchr16:27196893..27236095hg19UCSC Ensembl
Innerchr16:27104394..27143596hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3839203
hg1939203
hg1839203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060225
Supporting Variants
Samples
Known GenesKDM8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3549138
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer