A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016905



Internal ID19106122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5566131..5638934hg38UCSC Ensembl
Innerchr6:5566364..5639167hg19UCSC Ensembl
Innerchr6:5511363..5584166hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3872804
hg1972804
hg1872804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654741
Samples
Known GenesFARS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016905
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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