A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9564n54



Internal ID22777459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7417608..7478801hg38UCSC Ensembl
chr5:7417721..7478914hg19UCSC Ensembl
chr5:7470721..7531914hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3861194
hg1961194
hg1861194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596999, nsv597002, nsv597000
SamplesNINDS_14
Known GenesADCY2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9564n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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