A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047841



Internal ID18790372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46441715..46489856hg38UCSC Ensembl
Innerchr10:47055642..47108045hg19UCSC Ensembl
Innerchr10:46475648..46528051hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3848142
hg1952404
hg1852404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv806n100
Supporting Variantsnssv3705842
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)nsv1047841
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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