A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6734n54



Internal ID22774629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24490840..24492157hg38UCSC Ensembl
chr2:24713709..24715026hg19UCSC Ensembl
chr2:24567213..24568530hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg381318
hg191318
hg181318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv581193, nsv581194, nsv581192, nsv581189
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6734n54
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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