A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033436



Internal ID18775970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:22452539..22539307hg38UCSC Ensembl
Innerchr8:22310052..22396820hg19UCSC Ensembl
Innerchr8:22365997..22452765hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3886769
hg1986769
hg1886769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7137n100
Supporting Variantsnssv3685364
Samples
Known GenesPPP3CC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033436
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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