A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6526n100



Internal ID20158142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88521483..89890325hg38UCSC Ensembl
chr7:88150798..89519639hg19UCSC Ensembl
chr7:87988734..89357575hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg381368843
hg191368842
hg181368842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034860, nsv1029022
Samples
Known GenesC7orf62, ZNF804B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6526n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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