A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019692



Internal ID19108910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4684679..4716775hg38UCSC Ensembl
Innerchr7:4724310..4756406hg19UCSC Ensembl
Innerchr7:4690836..4722932hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3832097
hg1932097
hg1832097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655047
Samples
Known GenesFOXK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019692
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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