A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526031



Internal ID15106638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161907241..162333574hg38UCSC Ensembl
Innerchr6:162328273..162754606hg19UCSC Ensembl
Innerchr6:162248263..162674596hg18UCSC Ensembl
Innerchr6:162298684..162725017hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38426334
hg19426334
hg18426334
hg17426334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702262
Samples
Known GenesPARK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526031
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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