A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042362



Internal ID18784893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46407438..46472778hg38UCSC Ensembl
Innerchr10:47076675..47142310hg19UCSC Ensembl
Innerchr10:46496681..46562316hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3865341
hg1965636
hg1865636
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv819n100
Supporting Variantsnssv3511444, nssv3705931
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)nsv1042362
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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