A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015669



Internal ID19104887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:132803331..132860065hg38UCSC Ensembl
Innerchr8:133815576..133872310hg19UCSC Ensembl
Innerchr8:133884758..133941492hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3856735
hg1956735
hg1856735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691574
Samples
Known GenesPHF20L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015669
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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