A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522645



Internal ID15103252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52109491..52207217hg38UCSC Ensembl
Innerchr6:51974289..52072015hg19UCSC Ensembl
Innerchr6:52082248..52179974hg18UCSC Ensembl
Innerchr6:52082248..52179974hg17UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3897727
hg1997727
hg1897727
hg1797727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706045
Samples
Known GenesIL17A, MIR133B, MIR206
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522645
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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