A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695231



Internal ID18993512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:125964891..126099729hg38UCSC Ensembl
Innerchr9:128727170..128862008hg19UCSC Ensembl
Innerchr9:127766991..127901829hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38134839
hg19134839
hg18134839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054231
Supporting Variants
Samples
Known GenesPBX3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695231
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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