A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026922



Internal ID19116140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:93844167..94556093hg38UCSC Ensembl
Innerchr6:94553885..95265811hg19UCSC Ensembl
Innerchr6:94610606..95322532hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38711927
hg19711927
hg18711927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3751238
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)nsv1026922
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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