A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6744n100



Internal ID22792831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144255208..144378798hg38UCSC Ensembl
chr7:143952301..144075891hg19UCSC Ensembl
chr7:143583234..143706824hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38123591
hg19123591
hg18123591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025789, nsv1034322
Samples
Known GenesARHGEF34P, 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)dgv6744n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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