A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11007n54



Internal ID20144431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162163721..162165759hg38UCSC Ensembl
chr6:162584753..162586791hg19UCSC Ensembl
chr6:162504743..162506781hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg382039
hg192039
hg182039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605097, nsv605090, nsv605096, nsv605098, nsv605099, nsv605092, nsv605094, nsv605091, nsv605102, nsv605104, nsv605103
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11007n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss97
Observed Complex0
Frequencyn/a


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