A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043881



Internal ID19133100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46458897..46489856hg38UCSC Ensembl
Innerchr10:47055642..47090851hg19UCSC Ensembl
Innerchr10:46475648..46510857hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3830960
hg1935210
hg1835210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507426
Samples
Known GenesLOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043881
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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