A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3671151



Internal ID18622746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143870954..144214519hg38UCSC Ensembl
Innerchr7:143568047..143911612hg19UCSC Ensembl
Innerchr7:143198980..143542545hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38343566
hg19343566
hg18343566
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029035
Supporting Variants
Samples
Known GenesARHGEF35, CTAGE4, FAM115A, OR2A12, OR2A14, OR2A2, OR2A25, OR2A5, 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)nssv3671151
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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