A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017037



Internal ID18759572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161787295..161914435hg38UCSC Ensembl
Innerchr6:162208327..162335467hg19UCSC Ensembl
Innerchr6:162128317..162255457hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38127141
hg19127141
hg18127141
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6170n100
Supporting Variantsnssv3654536
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)nsv1017037
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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