A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6474n100



Internal ID20158090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76443262..76977978hg38UCSC Ensembl
chr7:76072579..76607295hg19UCSC Ensembl
chr7:75910515..76445231hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38534717
hg19534717
hg18534717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019262, nsv1022802, nsv1034345, nsv1021463, nsv1022937, nsv1019012, nsv1020797, nsv1034227, nsv1019183, nsv1025730, nsv1022194
Samples
Known GenesDTX2, FDPSP2, LOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6474n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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