A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046898



Internal ID18789429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:99349608..99401031hg38UCSC Ensembl
Innerchr9:102111890..102163313hg19UCSC Ensembl
Innerchr9:101151711..101203134hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3851424
hg1951424
hg1851424
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697573
Samples
Known GenesNAMA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046898
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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