A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008410



Internal ID18750941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248595945..248650779hg38UCSC Ensembl
Innerchr1:248759246..248814080hg19UCSC Ensembl
Innerchr1:246825869..246880703hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3854835
hg1954835
hg1854835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv635n100
Supporting Variantsnssv3495479, nssv3496803
Samples
Known GenesOR2T11, OR2T27, OR2T35
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008410
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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