A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6745n100



Internal ID22792832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144273205..144416681hg38UCSC Ensembl
chr7:143970298..144113774hg19UCSC Ensembl
chr7:143601231..143744707hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38143477
hg19143477
hg18143477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019601, nsv1033850
Samples
Known GenesARHGEF34P, ARHGEF5, NOBOX, OR2A1, OR2A20P, OR2A42, OR2A9P, 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)dgv6745n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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