A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3472411



Internal ID19064958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:79485089..79641217hg38UCSC Ensembl
Innerchr1:79950774..80106902hg19UCSC Ensembl
Innerchr1:79723362..79879490hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38156129
hg19156129
hg18156129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005022
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)nssv3472411
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