A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057110



Internal ID19146329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33342525..33389952hg38UCSC Ensembl
Innerchr17:31669543..31716970hg19UCSC Ensembl
Innerchr17:28693656..28741083hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3847428
hg1947428
hg1847428
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3561063
Samples
Known GenesASIC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057110
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