A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034810



Internal ID19124031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:132796688..132838352hg38UCSC Ensembl
Innerchr8:133808934..133850597hg19UCSC Ensembl
Innerchr8:133878116..133919779hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3841665
hg1941664
hg1841664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7321n100
Supporting Variantsnssv3691572
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)nsv1034810
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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