A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3750119



Internal ID19048400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:86035482..86616593hg38UCSC Ensembl
Innerchr6:86745200..87326311hg19UCSC Ensembl
Innerchr6:86801919..87383030hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38581112
hg19581112
hg18581112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027719
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)nssv3750119
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