A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3480949



Internal ID19069455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72284165..72343073hg38UCSC Ensembl
Innerchr1:72749848..72808756hg19UCSC Ensembl
Innerchr1:72522436..72581344hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3858909
hg1958909
hg1858909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001613
Supporting Variants
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)nssv3480949
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