A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052846



Internal ID18795377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92529627..92603827hg38UCSC Ensembl
Innerchr9:95291909..95366109hg19UCSC Ensembl
Innerchr9:94331730..94405930hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3874201
hg1974201
hg1874201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697556
Samples
Known GenesCENPP, ECM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052846
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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