A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033603



Internal ID18776136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161423234..161580404hg38UCSC Ensembl
Innerchr6:161844266..162001436hg19UCSC Ensembl
Innerchr6:161764256..161921426hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38157171
hg19157171
hg18157171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654529
Samples
Known GenesPARK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033603
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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