A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021884



Internal ID18764418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162251789..162412183hg38UCSC Ensembl
Innerchr6:162672821..162833215hg19UCSC Ensembl
Innerchr6:162592811..162753205hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38160395
hg19160395
hg18160395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6180n100
Supporting Variantsnssv3749592, nssv3654570
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)nsv1021884
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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