A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046906



Internal ID18789437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94236945..94477527hg38UCSC Ensembl
Innerchr9:96999227..97239809hg19UCSC Ensembl
Innerchr9:96039048..96279630hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38240583
hg19240583
hg18240583
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759787
Samples
Known GenesHIATL1, LOC100132077, NUTM2F, ZNF169
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046906
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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