A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033306



Internal ID18775840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162107008..162308495hg38UCSC Ensembl
Innerchr6:162528040..162729527hg19UCSC Ensembl
Innerchr6:162448030..162649517hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38201488
hg19201488
hg18201488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6175n100
Supporting Variantsnssv3654553
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)nsv1033306
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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