A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039444



Internal ID18781975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86653555..86714855hg38UCSC Ensembl
Innerchr10:88413312..88474612hg19UCSC Ensembl
Innerchr10:88403292..88464592hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3861301
hg1961301
hg1861301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv948n100
Supporting Variantsnssv3505939
Samples
Known GenesLDB3, OPN4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039444
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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