A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027056



Internal ID19116275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:6850970..6879511hg38UCSC Ensembl
Innerchr6:6851203..6879744hg19UCSC Ensembl
Innerchr6:6796202..6824743hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3828542
hg1928542
hg1828542
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747911
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)nsv1027056
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