A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518128



Internal ID15445421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100051488..100064292hg38UCSC Ensembl
Innerchr14:100517825..100530629hg19UCSC Ensembl
Innerchr14:99587578..99600382hg18UCSC Ensembl
Innerchr14:99587578..99600382hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3812805
hg1912805
hg1812805
hg1712805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv142n21
Supporting Variantsnssv695546
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518128
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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