A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6272n100



Internal ID20157888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12311969..12404864hg38UCSC Ensembl
chr7:12351595..12444490hg19UCSC Ensembl
chr7:12318120..12411015hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3892896
hg1992896
hg1892896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034475, nsv1029098, nsv1029941
Samples
Known GenesVWDE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6272n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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