A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017230



Internal ID18759765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:108994546..109061221hg38UCSC Ensembl
Innerchr6:109315749..109382424hg19UCSC Ensembl
Innerchr6:109422442..109489117hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3866676
hg1966676
hg1866676
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749509
Samples
Known GenesSESN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017230
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer