A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054381



Internal ID19143600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76836014..76885531hg38UCSC Ensembl
Innerchr9:79450930..79500447hg19UCSC Ensembl
Innerchr9:78640750..78690267hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3849518
hg1949518
hg1849518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696368
Samples
Known GenesPRUNE2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054381
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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