A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032369



Internal ID18774903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143604237..143686376hg38UCSC Ensembl
Innerchr6:143925374..144007513hg19UCSC Ensembl
Innerchr6:143967067..144049206hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3882140
hg1982140
hg1882140
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654453
Samples
Known GenesPHACTR2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032369
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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