A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036434



Internal ID18778965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46449118..46481988hg38UCSC Ensembl
Innerchr10:47067469..47100644hg19UCSC Ensembl
Innerchr10:46487475..46520650hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3832871
hg1933176
hg1833176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3502941
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)nsv1036434
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