A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015584



Internal ID18758118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170515957..170579200hg38UCSC Ensembl
Innerchr6:170825045..170888288hg19UCSC Ensembl
Innerchr6:170666970..170730213hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3863244
hg1963244
hg1863244
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3653098
Samples
Known GenesPDCD2, PSMB1, TBP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015584
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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