A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6536n100



Internal ID22792623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97756249..97793614hg38UCSC Ensembl
chr7:97385561..97422926hg19UCSC Ensembl
chr7:97223497..97260862hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3837366
hg1937366
hg1837366
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017302, nsv1034752
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)dgv6536n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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