A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516646



Internal ID15097253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1110830..1146101hg38UCSC Ensembl
Innerchr19:1110829..1146100hg19UCSC Ensembl
Innerchr19:1061829..1097100hg18UCSC Ensembl
Innerchr19:1061829..1097100hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3835272
hg1935272
hg1835272
hg1735272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658752, nssv673238, nssv657535, nssv670935, nssv687548, nssv669846, nssv685893, nssv673447, nssv680883, nssv680239, nssv672733, nssv685991, nssv693678, nssv677472, nssv655651
Samples
Known GenesSBNO2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516646
Frequency
Sample Size2026
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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