A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522675



Internal ID15449968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5725998..5732587hg38UCSC Ensembl
Innerchr6:5726231..5732820hg19UCSC Ensembl
Innerchr6:5671230..5677819hg18UCSC Ensembl
Innerchr6:5671230..5677819hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg386590
hg196590
hg186590
hg176590
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv369n21
Supporting Variantsnssv706081
Samples
Known GenesFARS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522675
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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