A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051268



Internal ID18793799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47003692..47142310hg19UCSC Ensembl
Innerchr10:46423698..46562316hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19138619
hg18138619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv781n100
Supporting Variantsnssv3515573, nssv3522664
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)nsv1051268
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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