A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015609



Internal ID18758143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162240826..162429877hg38UCSC Ensembl
Innerchr6:162661858..162850909hg19UCSC Ensembl
Innerchr6:162581848..162770899hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38189052
hg19189052
hg18189052
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749591
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)nsv1015609
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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