A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3490393



Internal ID19078034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196769481..196832708hg38UCSC Ensembl
Innerchr1:196738611..196801838hg19UCSC Ensembl
Innerchr1:195005234..195068461hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3863228
hg1963228
hg1863228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009598
Supporting Variants
Samples
Known GenesCFHR1, CFHR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3490393
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