A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031834



Internal ID18774368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162586362..162612734hg38UCSC Ensembl
Innerchr6:163007394..163033766hg19UCSC Ensembl
Innerchr6:162927384..162953756hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3826373
hg1926373
hg1826373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6193n100
Supporting Variantsnssv3655383, nssv3655384
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)nsv1031834
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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