A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052322



Internal ID18794853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46436509..46481242hg38UCSC Ensembl
Innerchr10:47068215..47113250hg19UCSC Ensembl
Innerchr10:46488221..46533256hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3844734
hg1945036
hg1845036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv814n100
Supporting Variantsnssv3519145
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)nsv1052322
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