A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031892



Internal ID18774426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161787295..161911062hg38UCSC Ensembl
Innerchr6:162208327..162332094hg19UCSC Ensembl
Innerchr6:162128317..162252084hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38123768
hg19123768
hg18123768
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6170n100
Supporting Variantsnssv3654535
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)nsv1031892
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