A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521411



Internal ID15448704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:134233200..134236251hg38UCSC Ensembl
Innerchr6:134554338..134557389hg19UCSC Ensembl
Innerchr6:134596031..134599082hg18UCSC Ensembl
Innerchr6:134596031..134599082hg17UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg383052
hg193052
hg183052
hg173052
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv395n21
Supporting Variantsnssv698021
Samples
Known GenesSGK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521411
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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