A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155104



Internal ID15527892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162068501..162185313hg38UCSC Ensembl
Innerchr6:162489533..162606345hg19UCSC Ensembl
Innerchr6:162409523..162526335hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38116813
hg19116813
hg18116813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605076
Supporting Variants
SamplesHGDP00556
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155104
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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