A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039572



Internal ID18782103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46446826..46489856hg38UCSC Ensembl
Innerchr10:47058780..47102936hg19UCSC Ensembl
Innerchr10:46478786..46522942hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3843031
hg1944157
hg1844157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv806n100
Supporting Variantsnssv3508564
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)nsv1039572
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