A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051273



Internal ID18793804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:53792127..53817783hg38UCSC Ensembl
Innerchr10:55551887..55577543hg19UCSC Ensembl
Innerchr10:55221893..55247549hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3825657
hg1925657
hg1825657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv861n100
Supporting Variantsnssv3513700
Samples
Known GenesPCDH15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051273
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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