A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047337



Internal ID18789868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92343356..92585202hg38UCSC Ensembl
Innerchr9:95105638..95347484hg19UCSC Ensembl
Innerchr9:94145459..94387305hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38241847
hg19241847
hg18241847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697553
Samples
Known GenesASPN, CENPP, ECM2, MIR4670, 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)nsv1047337
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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