A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043767



Internal ID19132986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47025092..47100644hg19UCSC Ensembl
Innerchr10:46445098..46520650hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg1975553
hg1875553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv791n100
Supporting Variantsnssv3507315
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)nsv1043767
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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