A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6361n100



Internal ID22792448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55536706..55569895hg38UCSC Ensembl
chr7:55604399..55637588hg19UCSC Ensembl
chr7:55571893..55605082hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3833190
hg1933190
hg1833190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022616, nsv1034564, nsv1022174, nsv1020892
Samples
Known GenesVOPP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6361n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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