A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6592n100



Internal ID22792679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116285309..116314039hg38UCSC Ensembl
chr7:115925363..115954093hg19UCSC Ensembl
chr7:115712599..115741329hg18UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg3828731
hg1928731
hg1828731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033025, nsv1024183
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)dgv6592n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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