A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049120



Internal ID18791651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46437212..46470757hg38UCSC Ensembl
Innerchr10:47078696..47112547hg19UCSC Ensembl
Innerchr10:46498702..46532553hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3833546
hg1933852
hg1833852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv820n100
Supporting Variantsnssv3519908
Samples
Known GenesLINC00842, 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)nsv1049120
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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