A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033222



Internal ID18775756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161918254..162281800hg38UCSC Ensembl
Innerchr6:162339286..162702832hg19UCSC Ensembl
Innerchr6:162259276..162622822hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38363547
hg19363547
hg18363547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6171n100
Supporting Variantsnssv3654541
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)nsv1033222
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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