A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053574



Internal ID19142793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87522560..87544690hg38UCSC Ensembl
Innerchr9:90137475..90159605hg19UCSC Ensembl
Innerchr9:89327295..89349425hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3822131
hg1922131
hg1822131
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697537
Samples
Known GenesDAPK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053574
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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