A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519424



Internal ID15446717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6345258..6346966hg38UCSC Ensembl
Innerchr10:6387220..6388928hg19UCSC Ensembl
Innerchr10:6427226..6428934hg18UCSC Ensembl
Innerchr10:6427226..6428934hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381709
hg191709
hg181709
hg171709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681777, nssv681186, nssv656136, nssv701137, nssv691151
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519424
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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