A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018573



Internal ID18761106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162604329..162751777hg38UCSC Ensembl
Innerchr6:163025361..163172809hg19UCSC Ensembl
Innerchr6:162945351..163092799hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38147449
hg19147449
hg18147449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655386
Samples
Known GenesPACRG, PARK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018573
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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