A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016831



Internal ID18759366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143728285..144369842hg38UCSC Ensembl
Innerchr7:143425378..144066935hg19UCSC Ensembl
Innerchr7:143056311..143697868hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38641558
hg19641558
hg18641558
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3670419
Samples
Known GenesARHGEF34P, ARHGEF35, ARHGEF5, CTAGE4, CTAGE6, CTAGE8, FAM115A, FAM115C, LOC154761, OR2A1, OR2A12, OR2A14, OR2A2, OR2A20P, OR2A25, OR2A42, OR2A5, OR2A7, OR2A9P, OR2F1, OR2F2, OR6B1, RNU6-57P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016831
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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