A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019742



Internal ID19108960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158300141..158371784hg38UCSC Ensembl
Innerchr7:158092833..158164476hg19UCSC Ensembl
Innerchr7:157785594..157857237hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3871644
hg1971644
hg1871644
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674738
Samples
Known GenesPTPRN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019742
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