A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517667



Internal ID15098274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16258599..16281352hg38UCSC Ensembl
Innerchr19:16369410..16392163hg19UCSC Ensembl
Innerchr19:16230410..16253163hg18UCSC Ensembl
Innerchr19:16230410..16253163hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3822754
hg1922754
hg1822754
hg1722754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679280, nssv653025, nssv658672, nssv689938, nssv676743, nssv682449, nssv677576, nssv692707, nssv657318, nssv655732, nssv652768, nssv654954, nssv684571, nssv673182
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517667
Frequency
Sample Size2026
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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