A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021844



Internal ID18764378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12356017..13444976hg38UCSC Ensembl
Innerchr9:12356017..13444975hg19UCSC Ensembl
Innerchr9:12346017..13434975hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381088960
hg191088959
hg181088959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690589
Samples
Known GenesFLJ41200, LURAP1L, MPDZ, TYRP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021844
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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