A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042166



Internal ID18784697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46395843..46464642hg38UCSC Ensembl
Innerchr10:47084773..47153919hg19UCSC Ensembl
Innerchr10:46504779..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3868800
hg1969147
hg1869147
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv819n100
Supporting Variantsnssv3505825, nssv3520767
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)nsv1042166
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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