A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049599



Internal ID18792130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92407857..92503276hg38UCSC Ensembl
Innerchr9:95170139..95265558hg19UCSC Ensembl
Innerchr9:94209960..94305379hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3895420
hg1995420
hg1895420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697555
Samples
Known GenesASPN, CENPP, ECM2, OMD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049599
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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