A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511922



Internal ID15504661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:162303263..162304933hg38UCSC Ensembl
Outerchr6:162724295..162725965hg19UCSC Ensembl
Outerchr6:162644285..162645955hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381671
hg191671
hg181671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624459
Samples1
Known GenesPARK2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511922
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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