A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045574



Internal ID18788105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46420071..46592975hg38UCSC Ensembl
Innerchr10:46956642..47129684hg19UCSC Ensembl
Innerchr10:46376648..46549690hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38172905
hg19173043
hg18173043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv764n100
Supporting Variantsnssv3515341
Samples
Known GenesGPRIN2, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045574
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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