A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016859



Internal ID18759394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:1459785..1645585hg38UCSC Ensembl
Innerchr6:1460020..1645819hg19UCSC Ensembl
Innerchr6:1405019..1590818hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38185801
hg19185800
hg18185800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654718
Samples
Known GenesFOXC1, GMDS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016859
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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