A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003097



Internal ID19092314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:208262669..208283580hg38UCSC Ensembl
Innerchr1:208436014..208456925hg19UCSC Ensembl
Innerchr1:206502637..206523548hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3820912
hg1920912
hg1820912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv566n100
Supporting Variantsnssv3491758, nssv3496361, nssv3500715
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)nsv1003097
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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