A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654718



Internal ID18606313
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 StatusS
Merged Variantsnsv1016859
Supporting Variants
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)nssv3654718
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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