A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009087



Internal ID19098305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177687443..177704487hg38UCSC Ensembl
Innerchr3:177405231..177422275hg19UCSC Ensembl
Innerchr3:178887925..178904969hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3817045
hg1917045
hg1817045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4998n100
Supporting Variantsnssv3738452
Samples
Known GenesLINC00578
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009087
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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