A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053460



Internal ID18795991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46441715..46489856hg38UCSC Ensembl
Innerchr10:47046997..47108045hg19UCSC Ensembl
Innerchr10:46467003..46528051hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3848142
hg1961049
hg1861049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv800n100
Supporting Variantsnssv3522481
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)nsv1053460
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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