A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035174



Internal ID19124393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11488714..11547571hg38UCSC Ensembl
Innerchr16:11582570..11641427hg19UCSC Ensembl
Innerchr16:11490071..11548928hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3858858
hg1958858
hg1858858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2729n100
Supporting Variantsnssv3557141
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035174
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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