A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10617n54



Internal ID22778512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34236508..34238257hg38UCSC Ensembl
chr6:34204285..34206034hg19UCSC Ensembl
chr6:34312263..34314012hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381750
hg191750
hg181750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602869, nsv602870, nsv602871, nsv602872
Samples
Known GenesHMGA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10617n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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