A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032779



Internal ID19122001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:132787493..132831134hg38UCSC Ensembl
Innerchr8:133799739..133843379hg19UCSC Ensembl
Innerchr8:133868921..133912561hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3843642
hg1943641
hg1843641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7319n100
Supporting Variantsnssv3691570
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)nsv1032779
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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