A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6228n100



Internal ID22792315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3696622..3799212hg38UCSC Ensembl
chr7:3736254..3838844hg19UCSC Ensembl
chr7:3702780..3805370hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38102591
hg19102591
hg18102591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031610, nsv1024704
Samples
Known GenesSDK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6228n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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