A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6725n100



Internal ID20158341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143870954..144214519hg38UCSC Ensembl
chr7:143568047..143911612hg19UCSC Ensembl
chr7:143198980..143542545hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38343566
hg19343566
hg18343566
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021409, nsv1029035
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)dgv6725n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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