A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075519



Internal ID15582019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162194574..162318733hg38UCSC Ensembl
Innerchr6:162615606..162739765hg19UCSC Ensembl
Innerchr6:162535596..162659755hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38124160
hg19124160
hg18124160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605116
Supporting Variants
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1075519
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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