A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025841



Internal ID18768373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162188687..162420402hg38UCSC Ensembl
Innerchr6:162609719..162841434hg19UCSC Ensembl
Innerchr6:162529709..162761424hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38231716
hg19231716
hg18231716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6177n100
Supporting Variantsnssv3654559
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)nsv1025841
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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