A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6728n100



Internal ID22792815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144172363..144369842hg38UCSC Ensembl
chr7:143869456..144066935hg19UCSC Ensembl
chr7:143500389..143697868hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38197480
hg19197480
hg18197480
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018201, nsv1023315
Samples
Known GenesARHGEF34P, ARHGEF35, ARHGEF5, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, 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)dgv6728n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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