A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029286



Internal ID19118505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:132800760..132838352hg38UCSC Ensembl
Innerchr8:133813006..133850597hg19UCSC Ensembl
Innerchr8:133882188..133919779hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3837593
hg1937592
hg1837592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7321n100
Supporting Variantsnssv3691573
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)nsv1029286
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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