A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525241



Internal ID15105848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:10544265..10563350hg38UCSC Ensembl
Innerchr2:10684391..10703476hg19UCSC Ensembl
Innerchr2:10601842..10620927hg18UCSC Ensembl
Innerchr2:10634989..10654074hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3819086
hg1919086
hg1819086
hg1719086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701331
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525241
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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