A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044044



Internal ID18786575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46411170..46572334hg38UCSC Ensembl
Innerchr10:46977283..47138582hg19UCSC Ensembl
Innerchr10:46397289..46558588hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38161165
hg19161300
hg18161300
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3705736, nssv3514377
Samples
Known GenesGPRIN2, HNRNPA1P33, 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)nsv1044044
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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