A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016570



Internal ID18759105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12576095..12722388hg38UCSC Ensembl
Innerchr9:12576095..12722387hg19UCSC Ensembl
Innerchr9:12566095..12712387hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38146294
hg19146293
hg18146293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690595
Samples
Known GenesTYRP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016570
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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