A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015617



Internal ID18758151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162586362..162612460hg38UCSC Ensembl
Innerchr6:163007394..163033492hg19UCSC Ensembl
Innerchr6:162927384..162953482hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3826099
hg1926099
hg1826099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6193n100
Supporting Variantsnssv3655382, nssv3655381
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)nsv1015617
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer