A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021504



Internal ID18764038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143887577..143945050hg38UCSC Ensembl
Innerchr7:143584670..143642143hg19UCSC Ensembl
Innerchr7:143215603..143273076hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3857474
hg1957474
hg1857474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3671152
Samples
Known GenesFAM115A, OR2F2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021504
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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