A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036859



Internal ID18779390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46428386..46482043hg38UCSC Ensembl
Innerchr10:47067414..47121369hg19UCSC Ensembl
Innerchr10:46487420..46541375hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3853658
hg1953956
hg1853956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv814n100
Supporting Variantsnssv3705897, nssv3705896
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)nsv1036859
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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