A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054737



Internal ID18797268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111562245..111612449hg38UCSC Ensembl
Innerchr9:114324525..114374729hg19UCSC Ensembl
Innerchr9:113364346..113414550hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3850205
hg1950205
hg1850205
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695048
Samples
Known GenesLRRC37A5P, PTGR1, ZNF483
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054737
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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