A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3705885



Internal ID18657480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46411170..46486346hg38UCSC Ensembl
Innerchr10:47063106..47138582hg19UCSC Ensembl
Innerchr10:46483112..46558588hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3875177
hg1975477
hg1875477
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040814
Supporting Variants
Samples
Known GenesHNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3705885
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