A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518227



Internal ID15445520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9753325..9768985hg38UCSC Ensembl
Innerchr2:9893454..9909114hg19UCSC Ensembl
Innerchr2:9810905..9826565hg18UCSC Ensembl
Innerchr2:9844052..9859712hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3815661
hg1915661
hg1815661
hg1715661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695654
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518227
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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