A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523810



Internal ID15451103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5727017..5732564hg38UCSC Ensembl
Innerchr6:5727250..5732797hg19UCSC Ensembl
Innerchr6:5672249..5677796hg18UCSC Ensembl
Innerchr6:5672249..5677796hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg385548
hg195548
hg185548
hg175548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv369n21
Supporting Variantsnssv699640
Samples
Known GenesFARS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523810
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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