A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051370



Internal ID18793901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:120810573..120906638hg38UCSC Ensembl
Innerchr9:123572851..123668916hg19UCSC Ensembl
Innerchr9:122612672..122708737hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3896066
hg1996066
hg1896066
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695218
Samples
Known GenesPHF19, PSMD5, PSMD5-AS1, TRAF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051370
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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