A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154688



Internal ID15532889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162311227..162524507hg38UCSC Ensembl
Innerchr6:162732259..162945539hg19UCSC Ensembl
Innerchr6:162652249..162865529hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38213281
hg19213281
hg18213281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605146
Supporting Variants
SamplesHGDP01397
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154688
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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