A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3463122



Internal ID18713319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8843872..8873183hg38UCSC Ensembl
Innerchr1:8903931..8933242hg19UCSC Ensembl
Innerchr1:8826518..8855829hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3829312
hg1929312
hg1829312
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001865
Supporting Variants
Samples
Known GenesENO1, MIR6728
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3463122
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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