A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038846



Internal ID18781377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46412752..46472778hg38UCSC Ensembl
Innerchr10:47076675..47136996hg19UCSC Ensembl
Innerchr10:46496681..46557002hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3860027
hg1960322
hg1860322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv818n100
Supporting Variantsnssv3705930
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)nsv1038846
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