A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6639n100



Internal ID22792726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136282664..136301340hg38UCSC Ensembl
chr7:135967412..135986088hg19UCSC Ensembl
chr7:135617952..135636628hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3818677
hg1918677
hg1818677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020516, nsv1028768, nsv1018347
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6639n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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