A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6698n100



Internal ID22792785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143119834..143203251hg38UCSC Ensembl
chr7:142816927..142900344hg19UCSC Ensembl
chr7:142527049..142610466hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3883418
hg1983418
hg1883418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034112, nsv1023470, nsv1016130, nsv1026139, nsv1019153, nsv1016175, nsv1018996, nsv1023242, nsv1022193, nsv1031431, nsv1020588, nsv1027804, nsv1020889, nsv1031198
Samples
Known GenesPIP, TAS2R39
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6698n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss235
Observed Complex0
Frequencyn/a


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