A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519127



Internal ID15099734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1308893..1324693hg38UCSC Ensembl
Innerchr10:1351088..1366888hg19UCSC Ensembl
Innerchr10:1341088..1356888hg18UCSC Ensembl
Innerchr10:1341088..1356888hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3815801
hg1915801
hg1815801
hg1715801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696605
Samples
Known GenesADARB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519127
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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