A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654715



Internal ID18952996
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 StatusS
Merged Variantsnsv1017614
Supporting Variants
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)nssv3654715
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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