A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058449



Internal ID19147668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6388017..6408236hg38UCSC Ensembl
Innerchr17:6291337..6311556hg19UCSC Ensembl
Innerchr17:6232061..6252280hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3820220
hg1920220
hg1820220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3094n100
Supporting Variantsnssv3560307
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)nsv1058449
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