A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655413



Internal ID18953694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167199775..167247175hg38UCSC Ensembl
Innerchr6:167613263..167660663hg19UCSC Ensembl
Innerchr6:167533253..167580653hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3847401
hg1947401
hg1847401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028537
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)nssv3655413
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