A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053205



Internal ID18795736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92356913..92420330hg38UCSC Ensembl
Innerchr9:95119195..95182612hg19UCSC Ensembl
Innerchr9:94159016..94222433hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3863418
hg1963418
hg1863418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697554
Samples
Known GenesCENPP, OGN, OMD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053205
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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