A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574345



Internal ID16361754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10268563..10297205hg38UCSC Ensembl
Innerchr17:10171880..10200522hg19UCSC Ensembl
Innerchr17:10112605..10141247hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3828643
hg1928643
hg1828643
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5444n54
Supporting Variantsnssv1149692
SamplesHGDP01305
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574345
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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