A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6301n100



Internal ID22792388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19164143..19181030hg38UCSC Ensembl
chr7:19203766..19220653hg19UCSC Ensembl
chr7:19170291..19187178hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3816888
hg1916888
hg1816888
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017453, nsv1024865
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)dgv6301n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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