A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648904



Internal ID18947185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:86081165..86653306hg38UCSC Ensembl
Innerchr6:86790883..87363024hg19UCSC Ensembl
Innerchr6:86847602..87419743hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38572142
hg19572142
hg18572142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029725
Supporting Variants
Samples
Known GenesMIR548AD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3648904
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