A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017614



Internal ID19106831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:1248415..1423267hg38UCSC Ensembl
Innerchr6:1248650..1423502hg19UCSC Ensembl
Innerchr6:1193650..1368501hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38174853
hg19174853
hg18174852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654715
Samples
Known GenesFOXF2, FOXQ1, MIR6720
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017614
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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